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 Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YDR519W | FPR2 | SGDID:S000002927 | FPR1 CAGL0K09724g |
FK506-binding protein 1 (FKBP) (EC 5.2.1.8) (Peptidyl-prolyl cis-trans isomerase) (PPIase) (Rapamycin-binding protein) |
5.2.1.8 | Candida glabrata | 5hua_a | Q6FMA3 | 99.00 | 1.20E-13 | 7.50E-18 | 78.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | PVX_101260 |
PVX_101260 |
5.2.1.8 | Plasmodium vivax | 2ki3_a | A5K8X6 | 98.80 | 6.40E-13 | 4.20E-17 | 77.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP13 FKBP22-1 FKBPK At5g45680 MRA19.7 |
Peptidyl-prolyl cis-trans isomerase FKBP13, chloroplastic (PPIase FKBP13) (EC 5.2.1.8) (FK506-binding protein 1) (FK506-binding protein 13) (AtFKBP13) (Immunophilin FKBP13) (Rotamase) |
5.2.1.8 | Arabidopsis thaliana | 1u79_c | Q9SCY2 | 99.00 | 6.70E-14 | 4.30E-18 | 82.10 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP1B FKBP12.6 FKBP1L FKBP9 OTK4 |
Peptidyl-prolyl cis-trans isomerase FKBP1B (PPIase FKBP1B) (EC 5.2.1.8) (12.6 kDa FK506-binding protein) (12.6 kDa FKBP) (FKBP-12.6) (FK506-binding protein 1B) (FKBP-1B) (Immunophilin FKBP12.6) (Rotamase) (h-FKBP-12) |
5.2.1.8 | Homo sapiens | Arrhythmogenic Right Ventricular Dysplasia, Familial, 2,Heart Disease,Hypertrophic Cardiomyopathy,Dilated Cardiomyopathy,Long Qt Syndrome,Malignant Hyperthermia,Heart Conduction Disease,Myasthenic Syndrome, Congenital, 5,Central Core Myopathy,Congenital Myasthenic Syndrome,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Brugada Syndrome,Arrhythmogenic Right Ventricular Dysplasia, Familial, 12,Ventricular Tachycardia, Catecholaminergic Polymorphic, 2,Long Qt Syndrome 1,Left Ventricular Noncompaction,Catecholaminergic Polymorphic Ventricular Tachycardia |
5l1d_b | P68106 | ENSG00000119782 | FKBP1B | 99.20 | 4.80E-15 | 3.10E-19 | 90.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR519W | FPR2 | SGDID:S000002927 | mip lpg0791 |
Outer membrane protein MIP (EC 5.2.1.8) (Macrophage infectivity potentiator) (Peptidyl-prolyl cis-trans isomerase) (PPIase) (Rotamase) |
5.2.1.8 | Legionella pneumophila | 2vcd_a | Q5ZXE0 | 98.80 | 9.20E-13 | 6.00E-17 | 77.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | tig MG238 |
Trigger factor (TF) (EC 5.2.1.8) (PPIase) |
5.2.1.8 | Mycoplasma genitalium | 1hxv_a | P47480 | 98.90 | 1.50E-13 | 9.70E-18 | 74.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP14 FKBP22 UNQ322/PRO381 |
Peptidyl-prolyl cis-trans isomerase FKBP14 (PPIase FKBP14) (EC 5.2.1.8) (22 kDa FK506-binding protein) (22 kDa FKBP) (FKBP-22) (FK506-binding protein 14) (FKBP-14) (Rotamase) |
5.2.1.8 | Homo sapiens | Myopathy,Cohen Syndrome,Bethlem Myopathy 1,Intracranial Hypotension,Morquio Syndrome,Postural Orthostatic Tachycardia Syndrome,Fkbp14 Kyphoscoliotic Ehlers-Danlos Syndrome,Hypermobile Ehlers-Danlos Syndrome,Collagen Disease,Kyphoscoliotic Ehlers-Danlos Syndrome,Ehlers-Danlos Syndrome,Muscular Dystrophy, Congenital, Lmna-Related,Blepharochalasis,Ciliary Dyskinesia, Primary, 6,Loeys-Dietz Syndrome,Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 2,Caspase 8 Deficiency,Scoliosis,Ullrich Congenital Muscular Dystrophy 1 |
4dip_d | Q9NWM8 | ENSG00000106080 | FKBP14 | 98.90 | 2.40E-13 | 1.60E-17 | 78.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR519W | FPR2 | SGDID:S000002927 | fkpA yzzS b3347 JW3309 |
FKBP-type peptidyl-prolyl cis-trans isomerase FkpA (PPIase) (EC 5.2.1.8) (Rotamase) |
5.2.1.8 | Escherichia coli | 1q6i_a | P45523 | 99.10 | 1.60E-14 | 1.10E-18 | 92.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP8 FKBP38 |
Peptidyl-prolyl cis-trans isomerase FKBP8 (PPIase FKBP8) (EC 5.2.1.8) (38 kDa FK506-binding protein) (38 kDa FKBP) (FKBP-38) (hFKBP38) (FK506-binding protein 8) (FKBP-8) (FKBPR38) (Rotamase) |
5.2.1.8 | Homo sapiens | Pineal Region Germinoma,Long Qt Syndrome 2,Neural Tube Defects |
2d9f_a | Q14318 | ENSG00000105701 | FKBP8 | 98.80 | 1.20E-12 | 7.80E-17 | 76.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR519W | FPR2 | SGDID:S000002927 | GL50803_0010450 GL50803_10450 |
GL50803_0010450 GL50803_10450 |
5.2.1.8 | Giardia intestinalis | 2lgo_a | Q8I6M8 | 98.80 | 8.60E-13 | 5.60E-17 | 77.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | AIP XAP2 |
AH receptor-interacting protein (AIP) (Aryl-hydrocarbon receptor-interacting protein) (HBV X-associated protein 2) (XAP-2) (Immunophilin homolog ARA9) |
Homo sapiens | Growth Hormone Secreting Pituitary Adenoma,Acroleukopathy, Symmetric,Pituitary Adenoma 1, Multiple Types,Pituitary Tumors,Adenoma,Hepatitis B,Acth-Secreting Pituitary Adenoma,Hepatitis,Familial Isolated Pituitary Adenoma,Pituitary Adenoma 4, Acth-Secreting,Hyperpituitarism,Acromegaly,Inherited Cancer-Predisposing Syndrome,Gigantism,Aip Familial Isolated Pituitary Adenomas,Carney Complex Variant,Silent Pituitary Adenoma,Null Pituitary Adenoma,Pituitary Gland Disease,Cancer-Associated Retinopathy,Functioning Pituitary Adenoma,Hormone Producing Pituitary Cancer,Multiple Endocrine Neoplasia,Primary Hyperparathyroidism,Pituitary Apoplexy,Pituitary Infarct,Pituitary Adenoma,Multiple Endocrine Neoplasia, Type Iv,Multiple Endocrine Neoplasia, Type I,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Cell Type Benign Neoplasm,Endocrine Organ Benign Neoplasm,Pituitary Adenoma, Prolactin-Secreting |
2lkn_a | O00170 | ENSG00000110711 | AIP | 98.90 | 6.00E-13 | 3.90E-17 | 81.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR519W | FPR2 | SGDID:S000002927 | FPR4 YLR449W L9324.3 |
FK506-binding protein 4 (EC 5.2.1.8) (Histone proline isomerase) (Peptidyl-prolyl cis-trans isomerase) (PPIase) (Rotamase) |
5.2.1.8 | Saccharomyces cerevisiae | 4bf8_a | Q06205 | 99.00 | 5.20E-14 | 3.40E-18 | 80.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | PSPTO_0135 |
PSPTO_0135 |
5.2.1.8 | Pseudomonas syringae | 5xb0_a | Q88B84 | 99.10 | 1.40E-14 | 9.00E-19 | 85.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | BDI_1692 |
BDI_1692 |
Parabacteroides distasonis | 4o2t_a | A6LCN0 | 98.80 | 6.90E-13 | 4.50E-17 | 81.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR519W | FPR2 | SGDID:S000002927 | FKBP3 FKBP25 |
Peptidyl-prolyl cis-trans isomerase FKBP3 (PPIase FKBP3) (EC 5.2.1.8) (25 kDa FK506-binding protein) (25 kDa FKBP) (FKBP-25) (FK506-binding protein 3) (FKBP-3) (Immunophilin FKBP25) (Rapamycin-selective 25 kDa immunophilin) (Rotamase) |
5.2.1.8 | Homo sapiens | 2mph_a | Q00688 | ENSG00000100442 | FKBP3 | 99.10 | 1.90E-14 | 1.20E-18 | 91.90 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR519W | FPR2 | SGDID:S000002927 | fbp BPSS1823 |
fbp BPSS1823 |
5.2.1.8 | Burkholderia pseudomallei | 2y78_a | Q63J95 | 98.90 | 4.50E-13 | 2.90E-17 | 78.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FDP41_012078 NF0084240 |
FDP41_012078 NF0084240 |
Naegleria fowleri | 6b4p_a | A0A2H4A315 | 98.80 | 1.50E-12 | 9.70E-17 | 75.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDR519W | FPR2 | SGDID:S000002927 | AIPL1 AIPL2 |
Aryl-hydrocarbon-interacting protein-like 1 |
Homo sapiens | Senior-Loken Syndrome 1,Exotropia,Retinitis Pigmentosa,Choroidal Dystrophy, Central Areolar, 1,Cone-Rod Dystrophy 12,Bardet-Biedl Syndrome,Leber Congenital Amaurosis 13,Leber Congenital Amaurosis 9,Pathologic Nystagmus,Hereditary Choroidal Atrophy,Eye Degenerative Disease,Partial Central Choroid Dystrophy,Retinal Vascular Disease,Leber Plus Disease,Retinal Degeneration,Cone-Rod Dystrophy 17,Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy,Fundus Dystrophy,Keratoconus,Color Blindness,Retinal Disease,Leber Congenital Amaurosis 14,Achromatopsia,Usher Syndrome, Type Iiia,Fraser Syndrome 3,Stargardt Disease,Pigmented Paravenous Chorioretinal Atrophy,Cone-Rod Dystrophy 2,Pseudopapilledema,Leber Congenital Amaurosis 3,Leber Congenital Amaurosis 12,Leber Congenital Amaurosis 6,Leber Congenital Amaurosis 7,Leber Congenital Amaurosis 8,Leber Congenital Amaurosis 11,Leber Congenital Amaurosis 15,Leber Congenital Amaurosis 4,Leber Congenital Amaurosis 5,Usher Syndrome,Cone-Rod Dystrophy 8,Congenital Stationary Night Blindness,Lissencephaly 3,Leber Congenital Amaurosis 16,Leber Congenital Amaurosis 10,Cone Dystrophy,Leber Congenital Amaurosis 1,Leber Congenital Amaurosis 2,Joubert Syndrome 1 |
5u9j_a | Q9NZN9 | ENSG00000129221 | AIPL1 | 99.10 | 1.80E-14 | 1.10E-18 | 88.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDR519W | FPR2 | SGDID:S000002927 | FKBP1A FKBP1 FKBP12 |
Peptidyl-prolyl cis-trans isomerase FKBP1A (PPIase FKBP1A) (EC 5.2.1.8) (12 kDa FK506-binding protein) (12 kDa FKBP) (FKBP-12) (Calstabin-1) (FK506-binding protein 1A) (FKBP-1A) (Immunophilin FKBP12) (Rotamase) |
5.2.1.8 | Homo sapiens | Amyotrophic Lateral Sclerosis 1,Subependymal Glioma,Benign Ependymoma,Subependymal Giant Cell Astrocytoma,Kidney Angiomyolipoma,Dilated Cardiomyopathy,Malignant Hyperthermia,Tuberous Sclerosis,Central Core Myopathy,Fibrodysplasia Ossificans Progressiva,Ventricular Tachycardia, Catecholaminergic Polymorphic, 2,Crouzon Syndrome With Acanthosis Nigricans,Exudative Vitreoretinopathy 6,Brachydactyly, Type A1, B,Left Ventricular Noncompaction |
2ppn_a | P62942 | ENSG00000088832 | FKBP1A | 98.90 | 4.30E-13 | 2.80E-17 | 75.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR519W | FPR2 | SGDID:S000002927 | BURPS1710b_A0907 |
BURPS1710b_A0907 |
5.2.1.8 | Burkholderia pseudomallei | 3uf8_a | Q3JK38 | 99.00 | 7.90E-14 | 5.10E-18 | 88.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP42 TWD1 UCU2 At3g21640 MIL23.21 |
Peptidyl-prolyl cis-trans isomerase FKBP42 (PPIase FKBP42) (EC 5.2.1.8) (42 kDa peptidyl-prolyl isomerase) (FK506-binding protein 42) (AtFKBP42) (Immunophilin FKBP42) (Protein TWISTED DWARF 1) (Protein ULTRACURVATA 2) (Rotamase) |
5.2.1.8 | Arabidopsis thaliana | 2f4e_a | Q9LDC0 | 99.00 | 5.40E-14 | 3.50E-18 | 86.90 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | RBP1 RBP11 CaO19.11186 CaO19.3702; RBP2 RBP12 CAALFM_C702570CA CaJ7.0299 CaO19.13810 CaO19.6452 |
FK506-binding protein 1 (FKBP) (EC 5.2.1.8) (Peptidyl-prolyl cis-trans isomerase) (PPIase) (Rapamycin-binding protein) |
5.2.1.8 | Candida albicans | 5i98_a | P28870 | 98.90 | 5.00E-13 | 3.30E-17 | 77.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP5 AIG6 FKBP51 |
Peptidyl-prolyl cis-trans isomerase FKBP5 (PPIase FKBP5) (EC 5.2.1.8) (51 kDa FK506-binding protein) (51 kDa FKBP) (FKBP-51) (54 kDa progesterone receptor-associated immunophilin) (Androgen-regulated protein 6) (FF1 antigen) (FK506-binding protein 5) (FKBP-5) (FKBP54) (p54) (HSP90-binding immunophilin) (Rotamase) |
5.2.1.8 | Homo sapiens | Acute Stress Disorder,Ocular Hypertension,Phobia, Specific,Post-Traumatic Stress Disorder,Major Depressive Disorder,Obsessive-Compulsive Disorder,Phobic Disorder,Borderline Personality Disorder,Dissociative Disorder,Bipolar Disorder,Prostate Cancer,Disease Of Mental Health,Personality Disorder,Endogenous Depression,Mental Depression,Corticosteroid-Binding Globulin Deficiency,Attention Deficit-Hyperactivity Disorder,Autism Spectrum Disorder,Anxiety,Rett Syndrome,Myelofibrosis,Asthma |
3o5q_a | Q13451 | ENSG00000096060 | FKBP5 | 98.80 | 1.40E-12 | 9.10E-17 | 76.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YDR519W | FPR2 | SGDID:S000002927 | FKBP35 PF3D7_1247400 |
Peptidyl-prolyl cis-trans isomerase FKBP35 (EC 5.2.1.8) (PfFKBP35) |
5.2.1.8 | Plasmodium falciparum | 4qt3_a | Q8I4V8 | 98.80 | 1.20E-12 | 7.60E-17 | 76.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | CIMG_08666 |
CIMG_08666 |
5.2.1.8 | Coccidioides immitis | 5b8i_c | J3K5Z5 | 98.80 | 1.00E-12 | 6.60E-17 | 76.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YDR519W | FPR2 | SGDID:S000002927 | FKBP4 FKBP52 |
Peptidyl-prolyl cis-trans isomerase FKBP4 (PPIase FKBP4) (EC 5.2.1.8) (51 kDa FK506-binding protein) (FKBP51) (52 kDa FK506-binding protein) (52 kDa FKBP) (FKBP-52) (59 kDa immunophilin) (p59) (FK506-binding protein 4) (FKBP-4) (FKBP59) (HSP-binding immunophilin) (HBI) (Immunophilin FKBP52) (Rotamase) [Cleaved into: Peptidyl-prolyl cis-trans isomerase FKBP4, N-terminally processed] |
5.2.1.8 | Homo sapiens | Acute Stress Disorder,Ocular Hypertension,Major Depressive Disorder,Sulfhemoglobinemia,Skin Atrophy,In Situ Carcinoma,Hypospadias,Disease Of Mental Health,Progesterone Resistance |
4lay_a | Q02790 | ENSG00000004478 | FKBP4 | 98.80 | 9.40E-13 | 6.10E-17 | 86.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |