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YDL126C CDC48 / SGDID:S000002284

SGD CSV

Yeast Systematic Name	Yeast Symbol	SGDID	Analog Name	Analog Description	EC	Organism	Disease	Structure	Uniprot	Human ID	Human Symbol	HHsearch Probability	HHsearch E_value	HHsearch P_value	HHsearch Score	Flag Disease related	Flag Homo sapiens	Flag Mus musculus	Flag Drosophila melanogaster	Flag Caenorhabditis elegans	Flag Arabidopsis thaliana
YDL126C	CDC48	SGDID:S000002284	PSMD13	26S proteasome non-ATPase regulatory subunit 13 (26S proteasome regulatory subunit RPN9) (26S proteasome regulatory subunit S11) (26S proteasome regulatory subunit p40.5)		Homo sapiens	Histrionic Personality Disorder	5vft_a	Q9UNM6	ENSG00000185627	PSMD13	98.70	1.90E-12	2.10E-16	133.50	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	vat Ta0840	VCP-like ATPase		Thermoplasma acidophilum		5g4f_c	O05209			99.90	1.50E-29	1.60E-33	288.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	RPT5 YTA1 YOR117W O3258 YOR3258W	26S proteasome regulatory subunit 6A (Tat-binding protein homolog 1) (TBP-1)		Saccharomyces cerevisiae		3whk_e	P33297			97.90	2.70E-09	3.30E-13	98.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PSMD2 TRAP2	26S proteasome non-ATPase regulatory subunit 2 (26S proteasome regulatory subunit RPN1) (26S proteasome regulatory subunit S2) (26S proteasome subunit p97) (Protein 55.11) (Tumor necrosis factor type 1 receptor-associated protein 2)		Homo sapiens	Angelman Syndrome,Cystic Fibrosis	6msb_f	Q13200	ENSG00000175166	PSMD2	99.10	1.20E-14	1.10E-18	159.20	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	FIGNL1	Fidgetin-like protein 1 (EC 3.6.4.-)	3.6.4.-	Homo sapiens		3d8b_a	Q6PIW4	ENSG00000132436	FIGNL1	99.10	9.20E-15	9.70E-19	152.30	0	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	MSMEG_0858	MSMEG_0858		Mycolicibacterium smegmatis		5e7p_a	A0QQS4			100.00	9.60E-42	9.90E-46	395.60	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	RPL26A RPL26 RPL33A YLR344W L8300.4	60S ribosomal protein L26-A (L33) (Large ribosomal subunit protein uL24-A) (YL33)		Saccharomyces cerevisiae		6r84_a	P05743			97.60	3.30E-08	3.90E-12	102.60	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	UFD1 PIP3 YGR048W	Ubiquitin fusion degradation protein 1 (UB fusion protein 1) (Polymerase-interacting protein 3)		Saccharomyces cerevisiae		1zc1_a	P53044			98.50	1.80E-11	1.70E-15	120.40	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	psmB AF_0481	Proteasome subunit beta (EC 3.4.25.1) (20S proteasome beta subunit) (Proteasome core protein PsmB)	3.4.25.1	Archaeoglobus fulgidus		6hea_i	Q9P996			98.10	1.20E-09	1.30E-13	111.30	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	MYCTH_2311706	MYCTH_2311706		Myceliophthora thermophila		5ubv_a	G2QPI5			98.00	2.20E-09	2.60E-13	97.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	MSP1 YTA4 YGR028W	Outer mitochondrial transmembrane helix translocase (EC 7.4.2.-) (Mitochondrial sorting of proteins) (Tat-binding homolog 4)	7.4.2.-	Saccharomyces cerevisiae		5w0t_a	P28737			97.90	4.80E-09	5.50E-13	102.10	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	mpa Rv2115c MTCY261.11c	Proteasome-associated ATPase (AAA ATPase forming ring-shaped complexes) (ARC) (Mycobacterial proteasome ATPase)		Mycobacterium tuberculosis		5kwa_a	P9WQN5			97.60	2.40E-08	2.60E-12	106.60	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	ftsH TTHA1492	ATP-dependent zinc metalloprotease FtsH (EC 3.4.24.-)	3.4.24.-	Thermus thermophilus		1iy2_a	Q5SI82			97.70	1.80E-08	2.10E-12	95.20	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	hisP STM2351	Histidine transport ATP-binding protein HisP		Salmonella typhimurium		1b0u_a	P02915			98.60	1.60E-11	1.40E-15	126.10	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	ftsH aq_936	ATP-dependent zinc metalloprotease FtsH (EC 3.4.24.-)	3.4.24.-	Aquifex aeolicus		6gcn_b	O67077			98.30	1.20E-10	1.30E-14	124.40	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PSMD8	26S proteasome non-ATPase regulatory subunit 8 (26S proteasome regulatory subunit RPN12) (26S proteasome regulatory subunit S14) (p31)		Homo sapiens	Cystic Fibrosis	5vfu_d	P48556	ENSG00000099341	PSMD8	98.70	1.60E-12	1.70E-16	134.30	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	SSO0287	SSO0287		Saccharolobus solfataricus		3ozx_b	Q980K5			97.80	7.00E-09	7.80E-13	110.40	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	CTHT_0002840	CTHT_0002840		Chaetomium thermophilum		6mat_b	G0RZG1			98.20	3.20E-10	3.30E-14	129.70	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PRE7 PRS3 PTS1 YBL041W YBL0407	Proteasome subunit beta type-6 (Multicatalytic endopeptidase complex subunit C5) (Proteasome component C5)	3.4.25.1	Saccharomyces cerevisiae		6fvy_m	P23724			99.30	1.20E-16	1.10E-20	174.30	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PSMC6 SUG2	26S proteasome regulatory subunit 10B (26S proteasome AAA-ATPase subunit RPT4) (Proteasome 26S subunit ATPase 6) (Proteasome subunit p42)		Homo sapiens	Alzheimer Disease,Cystic Fibrosis,Ehrlichiosis,Pheochromocytoma	5vfu_e	P62333	ENSG00000100519	PSMC6	98.80	6.60E-13	7.20E-17	136.10	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	pan MJ1176	Proteasome-activating nucleotidase (PAN) (Proteasomal ATPase) (Proteasome regulatory ATPase) (Proteasome regulatory particle)		Methanocaldococcus jannaschii		3h4m_a	Q58576			97.70	2.10E-08	2.50E-12	94.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	ftsH TM_0580	ATP-dependent zinc metalloprotease FtsH (EC 3.4.24.-)	3.4.24.-	Thermotoga maritima		2ce7_b	Q9WZ49			98.50	2.70E-11	2.90E-15	129.70	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	pan AF_1976	Proteasome-activating nucleotidase (PAN) (Proteasomal ATPase) (Proteasome regulatory ATPase) (Proteasome regulatory particle)		Archaeoglobus fulgidus		6he5_h	O28303			98.20	4.20E-10	4.70E-14	115.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PRE3 YJL001W J1407	Proteasome subunit beta type-1 (EC 3.4.25.1) (Macropain subunit PRE3) (Multicatalytic endopeptidase complex subunit PRE3) (Proteasome component PRE3) (Proteinase YSCE subunit PRE3)	3.4.25.1	Saccharomyces cerevisiae		6fvw_h	P38624			99.40	4.60E-17	4.30E-21	178.30	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	ABCF1 ABC50	ATP-binding cassette sub-family F member 1 (ATP-binding cassette 50) (TNF-alpha-stimulated ABC protein)		Homo sapiens	Autoimmune Pancreatitis,Bile Acid Synthesis Defect, Congenital, 5,Abcd Syndrome	5zxd_a	Q8NE71	ENSG00000204574	ABCF1	98.60	5.30E-12	5.80E-16	135.70	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	SCRG_02514	SCRG_02514		Saccharomyces cerevisiae		6az0_e	B3LL85			98.50	1.40E-11	1.50E-15	130.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PRP2 RNA2 YNR011C N2048	Pre-mRNA-splicing factor ATP-dependent RNA helicase-like protein PRP2 (EC 3.6.4.13) (Pre-mRNA-processing protein 2)	3.6.4.13	Saccharomyces cerevisiae		5gm6_y	P20095			97.70	1.40E-08	1.40E-12	118.10	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	VCP	Transitional endoplasmic reticulum ATPase (TER ATPase) (EC 3.6.4.6) (15S Mg(2+)-ATPase p97 subunit) (Valosin-containing protein) (VCP)	3.6.4.6	Homo sapiens	Muscular Disease,Amyotrophic Lateral Sclerosis 6 With Or Without Frontotemporal Dementia,Zellweger Syndrome,Supranuclear Palsy, Progressive, 1,Retinitis Pigmentosa,Myopathy,Myofibrillar Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Alzheimer Disease,Nominal Aphasia,Amyotrophic Lateral Sclerosis 1,Myositis,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Early-Onset, Autosomal Dominant Alzheimer Disease,Amyotrophic Lateral Sclerosis 8,Lateral Sclerosis,Motor Neuron Disease,Autosomal Dominant Limb-Girdle Muscular Dystrophy,Muscular Dystrophy,Movement Disease,Progressive Non-Fluent Aphasia,Dyscalculia,Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 1,Hereditary Spastic Paraplegia,Cystic Fibrosis,Machado-Joseph Disease,Spastic Paraplegia-Paget Disease Of Bone Syndrome,Adult-Onset Distal Myopathy Due To Vcp Mutation,Multisystem Proteinopathy,Dementia,Paget'S Disease Of Bone,Cockayne Syndrome,Alexia,Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 1,Charcot-Marie-Tooth Disease,Parkinson Disease, Late-Onset,Perry Syndrome,Speech And Communication Disorders,Progressive Muscular Atrophy,Tooth Disease,Pick Disease Of Brain,Werner Syndrome,Autosomal Dominant Cerebellar Ataxia,Neuronal Ceroid Lipofuscinosis,Mammary Paget'S Disease,Breast Adenocarcinoma,Disease Of Mental Health,Dementia, Lewy Body,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 6,Fanconi Anemia, Complementation Group G,Nonaka Myopathy,Alzheimer Disease 7,Amyotrophic Lateral Sclerosis 16, Juvenile,Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Aphasia,Writing Disorder,Inclusion Body Myositis,Associative Agnosia,Amyotrophic Lateral Sclerosis Type 6,Amyotrophic Lateral Sclerosis Type 14,Agraphia,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Frontotemporal Dementia,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7	5b6c_a	P55072	ENSG00000165280	VCP	98.00	1.70E-09	1.80E-13	98.80	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	TRIP13 PCH2	Pachytene checkpoint protein 2 homolog (Human papillomavirus type 16 E1 protein-binding protein) (16E1-BP) (HPV16 E1 protein-binding protein) (Thyroid hormone receptor interactor 13) (Thyroid receptor-interacting protein 13) (TR-interacting protein 13) (TRIP-13)		Homo sapiens	Pontocerebellar Hypoplasia, Type 3,Mosaic Variegated Aneuploidy Syndrome,Choreatic Disease,Mosaic Variegated Aneuploidy Syndrome 3,Microcephaly,Pontocerebellar Hypoplasia, Type 4,Pontocerebellar Hypoplasia, Type 2a,Pontocerebellar Hypoplasia, Type 5,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,Mosaic Variegated Aneuploidy Syndrome 2,Wilms Tumor 1,Pontocerebellar Hypoplasia,Oocyte Maturation Defect 9,Lung Cancer	6f0x_e	Q15645			97.80	6.70E-09	6.80E-13	110.50	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	SPG7 CAR CMAR PGN	Paraplegin (EC 3.4.24.-) (Cell matrix adhesion regulator) (Spastic paraplegia 7 protein)	3.4.24.-	Homo sapiens	Paraplegia,Spastic Paraplegia 42, Autosomal Dominant,Neuropathy, Hereditary Motor And Sensory, Type Via, With Optic Atrophy,Seizure Disorder,Spasticity,Optic Nerve Disease,Spinocerebellar Ataxia, Autosomal Recessive 24,Mitochondrial Myopathy,Spastic Paraplegia 50, Autosomal Recessive,Spinal Muscular Atrophy,Hereditary Spastic Paraplegia 30,Hereditary Spastic Paraplegia 51,Hereditary Spastic Paraplegia 72,Secondary Hyperparathyroidism,Spastic Paraplegia 17, Autosomal Dominant,Spastic Paraplegia 15, Autosomal Recessive,Proximal Spinal Muscular Atrophy,Chronic Progressive External Ophthalmoplegia,Spastic Paraplegia 5a, Autosomal Recessive,Spastic Paraplegia 56, Autosomal Recessive,Spastic Paraplegia 49, Autosomal Recessive,Spastic Paraplegia 54, Autosomal Recessive,Spastic Paraplegia 55, Autosomal Recessive,Hereditary Spastic Paraplegia,Motor Peripheral Neuropathy,Ocular Motility Disease,Complex Hereditary Spastic Paraplegia,Mitochondrial Complex Iii Deficiency, Nuclear Type 2,Optic Atrophy 3, Autosomal Dominant,Optic Atrophy 1,Spastic Paraparesis,Cerebellar Disease,Mitochondrial Disorders,Neuropathy,Cranial Nerve Disease,Spastic Paraplegia 20, Autosomal Recessive,Early Myoclonic Encephalopathy,Peripheral Nervous System Disease,Polyneuropathy,Spinocerebellar Ataxia, Autosomal Recessive 14,Spastic Paraplegia 28, Autosomal Recessive,Autosomal Dominant Cerebellar Ataxia,Hypoparathyroidism,Spastic Paraplegia 48, Autosomal Recessive,Spastic Paraplegia 8, Autosomal Dominant,Hutchinson-Gilford Progeria Syndrome,Disease Of Mental Health,Spinocerebellar Ataxia 28,Spastic Paraplegia 31, Autosomal Dominant,Spastic Paraplegia 16, X-Linked,Spastic Paraplegia 63, Autosomal Recessive,Spastic Paraplegia 10, Autosomal Dominant,Dentatorubral-Pallidoluysian Atrophy,Spastic Paraplegia 11, Autosomal Recessive,Optic Atrophy 5,Spastic Paraplegia 14, Autosomal Recessive,Spastic Paraplegia 3, Autosomal Dominant,Spastic Paraplegia 47, Autosomal Recessive,Spastic Paraplegia 4, Autosomal Dominant,Spastic Paraplegia 13, Autosomal Dominant,Spastic Paraplegia 18, Autosomal Recessive,Spastic Paraplegia 32, Autosomal Recessive,Primary Lateral Sclerosis, Adult, 1,Spastic Paraplegia 39, Autosomal Recessive,Optic Atrophy 9,Spastic Paraplegia 46, Autosomal Recessive,Spastic Paraplegia 35, Autosomal Recessive,Perrault Syndrome,Masa Syndrome,Spastic Ataxia 5,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,Spastic Paraplegia 7, Autosomal Recessive,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Leber Hereditary Optic Neuropathy, Modifier Of,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Spastic Paraplegia 2, X-Linked,Familial Hypocalciuric Hypercalcemia,Behr Syndrome,Kearns-Sayre Syndrome,Spastic Paraplegia 6, Autosomal Dominant,3-Methylglutaconic Aciduria, Type Iii	2qz4_a	Q9UQ90	ENSG00000197912	SPG7	97.80	7.20E-09	8.70E-13	95.10	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	NVL NVL2	Nuclear valosin-containing protein-like (NVLp) (Nuclear VCP-like protein)		Homo sapiens	Cone-Rod Dystrophy 2,Charcot-Marie-Tooth Disease, Axonal, Type 2e	2x8a_a	O15381	ENSG00000143748	NVL	98.10	8.00E-10	9.30E-14	105.00	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	RPT1 CIM5 YTA3 YKL145W	26S proteasome regulatory subunit 7 homolog (Protein CIM5) (Tat-binding homolog 3)		Saccharomyces cerevisiae		4jpo_c	P33299			97.90	3.50E-09	3.80E-13	88.40	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	TER94 VCP CG2331	Transitional endoplasmic reticulum ATPase TER94 (EC 3.6.4.6) (Valosin-containing protein homolog)	3.6.4.6	Drosophila melanogaster		4rv0_e	Q7KN62			98.20	4.40E-10	4.90E-14	102.50	0	0	0	1	0	0
YDL126C	CDC48	SGDID:S000002284	Msed_1672	Msed_1672		Metallosphaera sedula		4d81_a	A4YHC5			97.60	3.00E-08	3.70E-12	91.60	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	RCA At2g39730 T5I7.3	Ribulose bisphosphate carboxylase/oxygenase activase, chloroplastic (RA) (RuBisCO activase)		Arabidopsis thaliana		4w5w_a	P10896			98.10	1.20E-09	1.30E-13	113.90	0	0	0	0	0	1
YDL126C	CDC48	SGDID:S000002284	RPT4 CRL13 PCS1 SUG2 YOR259C	26S proteasome subunit RPT4 (26S protease subunit SUG2) (Proteasomal cap subunit)		Saccharomyces cerevisiae		6ef0_l	P53549			98.00	1.40E-09	1.70E-13	101.70	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	SPAST ADPSP FSP2 KIAA1083 SPG4	Spastin (EC 5.6.1.1) (Spastic paraplegia 4 protein)	5.6.1.1	Homo sapiens	Paraplegia,Chromosome 1q21.1 Duplication Syndrome,Dystonia 9,Spastic Paraplegia 42, Autosomal Dominant,Zellweger Syndrome,Seizure Disorder,Spasticity,Amyotrophic Lateral Sclerosis 1,Motor Neuron Disease,Hereditary Spastic Paraplegia 30,Hereditary Spastic Paraplegia 72,Spastic Paraplegia 17, Autosomal Dominant,Spastic Paraplegia 15, Autosomal Recessive,Spastic Paraplegia 5a, Autosomal Recessive,Spastic Paraplegia 56, Autosomal Recessive,Hereditary Spastic Paraplegia,Spastic Paraplegia 43, Autosomal Recessive,Pure Hereditary Spastic Paraplegia,Spastic Paraparesis,Spastic Paraplegia 4,Chromosome 17p13.3, Centromeric, Duplication Syndrome,Spastic Paraplegia 26, Autosomal Recessive,Spastic Paraplegia 20, Autosomal Recessive,Spastic Paraplegia 41, Autosomal Dominant,Spastic Diplegia,Spastic Paraplegia 48, Autosomal Recessive,Spastic Paraplegia 8, Autosomal Dominant,Disease Of Mental Health,Spastic Paraplegia 33, Autosomal Dominant,Spastic Paraplegia 31, Autosomal Dominant,Neuropathy, Hereditary Sensory, Type Id,Spastic Paraplegia 16, X-Linked,Spastic Paraplegia 61, Autosomal Recessive,Spastic Paraplegia 10, Autosomal Dominant,Spastic Paraplegia 11, Autosomal Recessive,Spastic Paraplegia 12, Autosomal Dominant,Spastic Paraplegia 14, Autosomal Recessive,Spastic Paraplegia 3, Autosomal Dominant,Spastic Paraplegia 47, Autosomal Recessive,Spastic Paraplegia 4, Autosomal Dominant,Spastic Paraplegia 13, Autosomal Dominant,Myopathy, Proximal, With Ophthalmoplegia,Spastic Paraplegia 39, Autosomal Recessive,Spastic Paraplegia 46, Autosomal Recessive,Masa Syndrome,Charcot-Marie-Tooth Disease, Axonal, Type 2e,Spastic Paraplegia 2, X-Linked,Spastic Paraplegia 6, Autosomal Dominant	5z6r_a	Q9UBP0	ENSG00000021574	SPAST	99.00	6.20E-14	6.30E-18	148.90	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PSMD14 POH1	26S proteasome non-ATPase regulatory subunit 14 (EC 3.4.19.-) (26S proteasome regulatory subunit RPN11) (26S proteasome-associated PAD1 homolog 1)	3.4.19.-	Homo sapiens	Angelman Syndrome,Cystic Fibrosis,Autosomal Dominant Cerebellar Ataxia	5vft_c	O00487	ENSG00000115233	PSMD14	98.10	6.60E-10	7.60E-14	112.10	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PRE2 DOA3 PRG1 YPR103W P8283.10	Proteasome subunit beta type-5 (EC 3.4.25.1) (Macropain subunit PRE2) (Multicatalytic endopeptidase complex subunit PRE2) (Proteasome component PRE2) (Proteinase YSCE subunit PRE2)	3.4.25.1	Saccharomyces cerevisiae		5mp9_l	P30656			98.60	1.20E-11	1.30E-15	130.70	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	RPT6 CIM3 CRL3 SUG1 TBPY TBY1 YGL048C	26S proteasome regulatory subunit 8 homolog (Protein CIM3) (Protein SUG1) (Tat-binding protein TBY1)		Saccharomyces cerevisiae		6ef1_j	Q01939			97.90	3.90E-09	4.70E-13	98.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	Dhx37	Dhx37		Mus musculus		6o16_a	Q6NZL1			97.30	1.60E-07	1.60E-11	109.60	0	0	1	0	0	0
YDL126C	CDC48	SGDID:S000002284	mel	mel		Pseudomonas aeruginosa		5zlu_ee	A0A1I9WCL8			98.50	1.40E-11	1.50E-15	129.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	VPS4B SKD1 VPS42 MIG1	Vacuolar protein sorting-associated protein 4B (EC 3.6.4.6) (Cell migration-inducing gene 1 protein) (Suppressor of K(+) transport growth defect 1) (Protein SKD1)	3.6.4.6	Homo sapiens	Parotid Gland Cancer,Submandibular Gland Cancer,Dentin Dysplasia,Submandibular Gland Disease,Dentin Dysplasia, Type I	1xwi_a	O75351	ENSG00000119541	VPS4B	98.90	2.80E-13	3.10E-17	136.00	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	VPS4 CSC1 DID6 END13 GRD13 VPL4 VPT10 YPR173C P9705.10	Vacuolar protein sorting-associated protein 4 (DOA4-independent degradation protein 6) (Protein END13) (Vacuolar protein-targeting protein 10)		Saccharomyces cerevisiae		3eie_a	P52917			98.80	8.20E-13	9.10E-17	132.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	KATNAL1	Katanin p60 ATPase-containing subunit A-like 1 (Katanin p60 subunit A-like 1) (EC 5.6.1.1) (p60 katanin-like 1)	5.6.1.1	Homo sapiens	13q12.3 Microdeletion Syndrome,Microcephaly,Hypertrichosis Universalis Congenita, Ambras Type,Gluten Allergy,Joubert Syndrome 26	6b5c_a	Q9BW62	ENSG00000102781	KATNAL1	98.50	2.80E-11	3.20E-15	118.40	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	Uncharacterized protein	Uncharacterized protein		Oryctolagus cuniculus		5lzv_jj	G1SG72			97.50	7.60E-08	8.60E-12	102.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PUP1 YOR157C	Proteasome subunit beta type-2 (EC 3.4.25.1) (Macropain subunit PUP1) (Multicatalytic endopeptidase complex subunit PUP1) (Proteasome component PUP1) (Proteinase YSCE subunit PUP1)	3.4.25.1	Saccharomyces cerevisiae		6fvt_i	P25043			98.80	5.30E-13	5.50E-17	140.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	ftsH HP_1069	ATP-dependent zinc metalloprotease FtsH (EC 3.4.24.-)	3.4.24.-	Helicobacter pylori		2r65_b	P71408			97.70	2.00E-08	2.40E-12	93.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	Pex1	Peroxisome biogenesis factor 1 (Peroxin-1)		Mus musculus		1wlf_a	Q5BL07			98.00	2.40E-09	2.50E-13	99.80	0	0	1	0	0	0
YDL126C	CDC48	SGDID:S000002284	AFG3L2	AFG3-like protein 2 (EC 3.4.24.-) (Paraplegin-like protein)	3.4.24.-	Homo sapiens	Progressive Myoclonus Epilepsy,Dystonia 9,Spasticity,Epilepsy,Optic Nerve Disease,Episodic Ataxia,Chronic Progressive External Ophthalmoplegia,Hereditary Spastic Paraplegia,Cerebellar Ataxia Type 41,Cerebellar Ataxia Type 48,Choreatic Disease,Sensorineural Hearing Loss,Spastic Paraparesis,Cerebellar Disease,Dystonia,Neuropathy,Early Myoclonic Encephalopathy,Spinocerebellar Ataxia 30,Spinocerebellar Ataxia, Autosomal Recessive 14,Myoclonus,Spinocerebellar Ataxia 29,Alacrima, Achalasia, And Mental Retardation Syndrome,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Spinocerebellar Ataxia 28,Optic Atrophy With Or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, And Neuropathy,Dentatorubral-Pallidoluysian Atrophy,Aceruloplasminemia,Optic Atrophy 5,Spinocerebellar Ataxia, Autosomal Recessive 8,Optic Atrophy 9,Spinocerebellar Ataxia 15,Perrault Syndrome,Spastic Ataxia 5, Autosomal Recessive,Spastic Ataxia 4,Spastic Ataxia 5,Hereditary Ataxia,Spastic Ataxia,Spastic Paraplegia 7, Autosomal Recessive,Spinocerebellar Ataxia 21,Spinocerebellar Ataxia 18,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Optic Atrophy 10 With Or Without Ataxia, Mental Retardation, And Seizures,Ptosis,Optic Atrophy 12,Striatal Degeneration, Autosomal Dominant 2,Kearns-Sayre Syndrome,3-Methylglutaconic Aciduria, Type Iii	6nyy_b	Q9Y4W6	ENSG00000141385	AFG3L2	98.80	6.20E-13	6.10E-17	147.20	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	pan PH0201	Proteasome-activating nucleotidase (PAN) (Proteasomal ATPase) (Proteasome regulatory ATPase) (Proteasome regulatory particle)		Pyrococcus horikoshii		5eqt_a	O57940			97.70	1.80E-08	2.20E-12	92.10	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	vmlR expZ BSU05610	Ribosome protection protein VmlR (Multidrug resistance system ATP-binding protein VmlR)		Bacillus subtilis		6ha8_v	P39115			97.80	1.20E-08	1.20E-12	110.10	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	UFD1 UFD1L	Ubiquitin recognition factor in ER-associated degradation protein 1 (Ubiquitin fusion degradation protein 1) (UB fusion protein 1)		Homo sapiens	Chromosome 22q11.2 Duplication Syndrome,Multisystem Proteinopathy,Patent Foramen Ovale,Tetralogy Of Fallot,Digeorge Syndrome,Velocardiofacial Syndrome,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia,Chromosomal Deletion Syndrome	2yuj_a	Q92890	ENSG00000070010	UFD1	98.10	8.50E-10	8.40E-14	106.00	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	Ahos_1335	Ahos_1335		Acidianus hospitalis		4lcb_a	F4B4B0			98.60	1.20E-11	1.40E-15	125.00	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PRE1 YER012W	Proteasome subunit beta type-4 (Macropain subunit C11) (Multicatalytic endopeptidase complex subunit C11) (Proteasome component C11) (Proteinase YSCE subunit 11)	3.4.25.1	Saccharomyces cerevisiae		6fvt_k	P22141			98.80	5.60E-13	5.90E-17	139.80	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	SEM1 C7orf76 DSS1 SHFDG1 SHFM1	26S proteasome complex subunit SEM1 (26S proteasome complex subunit DSS1) (Deleted in split hand/split foot protein 1) (Split hand/foot deleted protein 1) (Split hand/foot malformation type 1 protein)		Homo sapiens	Eyelid Carcinoma,Orofacial Cleft 4,Split Hand-Foot Malformation,Isolated Split Hand-Split Foot Malformation,Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss, Autosomal Recessive,Skin Squamous Cell Carcinoma,Split-Hand/Foot Malformation 6,Paranoid Personality Disorder,Shoulder Impingement Syndrome,Fanconi Anemia, Complementation Group A,Split-Hand/Foot Malformation 4,Split-Hand/Foot Malformation 1,Citrullinemia, Type Ii, Neonatal-Onset,Chromosome 2q35 Duplication Syndrome,Split-Hand/Foot Malformation 5,Split-Hand/Foot Malformation 3,Attention Deficit-Hyperactivity Disorder,Split-Hand/Foot Malformation 2	6msb_e	P60896	ENSG00000127922	SEM1	98.40	3.80E-11	4.10E-15	125.10	1	1	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	RCA1	Ribulose bisphosphate carboxylase/oxygenase activase 1, chloroplastic (RA 1) (RuBisCO activase 1)		Nicotiana tabacum		3t15_a	Q40460			97.90	4.50E-09	4.50E-13	106.70	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PAB0824	PAB0824		Pyrococcus abyssi		3bk7_a	Q9UZA4			98.20	3.20E-10	3.50E-14	123.50	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	figl-1 F32D1.1	Fidgetin-like protein 1 (EC 3.6.4.-) (Fidgetin homolog)	3.6.4.-	Caenorhabditis elegans		4l15_a	O16299			98.60	6.60E-12	7.30E-16	126.40	0	0	0	0	1	0
YDL126C	CDC48	SGDID:S000002284	mei-1 T01G9.5	Meiotic spindle formation protein mei-1 (EC 5.6.1.1) (Katanin p60 ATPase-containing subunit A1) (Katanin p60 subunit A1) (p60 katanin)	5.6.1.1	Caenorhabditis elegans		6b5d_a	P34808			98.40	5.10E-11	5.80E-15	117.20	0	0	0	0	1	0
YDL126C	CDC48	SGDID:S000002284	spas CG5977	Spastin (EC 5.6.1.1) (D-Spastin) (Dm-Spastin) (Dspastin)	5.6.1.1	Drosophila melanogaster		3b9p_a	Q8I0P1			98.10	5.50E-10	6.40E-14	107.40	0	0	0	1	0	0
YDL126C	CDC48	SGDID:S000002284	mpa MRA_2130	Proteasome-associated ATPase (AAA ATPase forming ring-shaped complexes) (ARC) (Mycobacterial proteasome ATPase)		Mycobacterium tuberculosis		5kzf_k	A5U4E1			97.70	1.30E-08	1.40E-12	109.80	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	YEF3 EFC1 TEF3 YEF3A YLR249W L9672.5	Elongation factor 3A (EF-3) (EF-3A) (EC 3.6.4.-) (Eukaryotic elongation factor 3) (eEF3) (Translation elongation factor 3A) (Yeast elongation factor 3)	3.6.4.-	Saccharomyces cerevisiae		2iw3_a	P16521			97.40	8.60E-08	9.90E-12	107.90	0	0	0	0	0	0
YDL126C	CDC48	SGDID:S000002284	PSMD4 MCB1	26S proteasome non-ATPase regulatory subunit 4 (26S proteasome regulatory subunit RPN10) (26S proteasome regulatory subunit S5A) (Antisecretory factor 1) (AF) (ASF) (Multiubiquitin chain-binding protein)		Homo sapiens	Alzheimer Disease,Angelman Syndrome,Cystic Fibrosis,Cholera,Encephalopathy, Familial, With Neuroserpin Inclusion Bodies,Inflammatory Bowel Disease	5vft_b	P55036	ENSG00000159352	PSMD4	98.80	1.30E-12	1.40E-16	133.80	1	1	0	0	0	0