







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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YOR290C | SNF2 | SGDID:S000005816 | vas vasa CG46283 |
ATP-dependent RNA helicase vasa (EC 3.6.4.13) (Antigen Mab46F11) |
3.6.4.13 | Drosophila melanogaster | 2db3_b | P09052 | 99.30 | 2.10E-16 | 2.40E-20 | 177.90 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | RAD26 GTA1085 YJR035W J1606 |
DNA repair and recombination protein RAD26 (EC 3.6.4.12) (ATP-dependent helicase RAD26) |
3.6.4.12 | Saccharomyces cerevisiae | 5vvr_m | P40352 | 99.90 | 3.10E-27 | 2.90E-31 | 309.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | PF2015 |
PF2015 |
Pyrococcus furiosus | 1wp9_a | Q8TZH8 | 99.40 | 5.40E-18 | 6.70E-22 | 187.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | Dcr-2 cg6493 Dcr dcr DCR-2 dcr-2 Dcr-2-RA DCR2 Dcr2 dcr2 dDcr2 dic2 DICER Dicer dicer DICER-2 dicer-2 Dicer2 dicer2 dmDcr-2 Dmel\CG6493 CG6493 Dmel_CG6493 |
Dcr-2 cg6493 Dcr dcr DCR-2 dcr-2 Dcr-2-RA DCR2 Dcr2 dcr2 dDcr2 dic2 DICER Dicer dicer DICER-2 dicer-2 Dicer2 dicer2 dmDcr-2 Dmel\CG6493 CG6493 Dmel_CG6493 |
3.1.21.1,3.1.26.-,3.1.26.3,3.6.1.3, | Drosophila melanogaster | 6bu9_a | A1ZAW0 | 99.20 | 1.70E-15 | 1.70E-19 | 205.20 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | PRP5 RNA5 YBR237W YBR1603 |
Pre-mRNA-processing ATP-dependent RNA helicase PRP5 (EC 3.6.4.13) |
3.6.4.13 | Saccharomyces cerevisiae | 4ljy_a | P21372 | 99.40 | 7.90E-18 | 9.00E-22 | 194.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | SWR1 YDR334W D9651.6 |
Helicase SWR1 (EC 3.6.4.12) (Swi2/Snf2-related 1) |
3.6.4.12 | Saccharomyces cerevisiae | 6gej_m | Q05471 | 99.90 | 9.90E-30 | 9.00E-34 | 340.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | MYCTH_115909 |
MYCTH_115909 |
Myceliophthora thermophila | 5hzr_a | G2QDW1 | 100.00 | 2.60E-55 | 2.70E-59 | 550.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | POLQ POLH |
DNA polymerase theta (EC 2.7.7.7) (DNA polymerase eta) |
2.7.7.7 | Homo sapiens | Interdigitating Dendritic Cell Sarcoma,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A |
5aga_a | O75417 | ENSG00000051341 | POLQ | 99.20 | 1.30E-15 | 1.40E-19 | 191.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | EIF4A3 DDX48 KIAA0111 |
Eukaryotic initiation factor 4A-III (eIF-4A-III) (eIF4A-III) (EC 3.6.4.13) (ATP-dependent RNA helicase DDX48) (ATP-dependent RNA helicase eIF4A-3) (DEAD box protein 48) (Eukaryotic initiation factor 4A-like NUK-34) (Eukaryotic translation initiation factor 4A isoform 3) (Nuclear matrix protein 265) (NMP 265) (hNMP 265) [Cleaved into: Eukaryotic initiation factor 4A-III, N-terminally processed] |
3.6.4.13 | Homo sapiens | Metaphyseal Chondrodysplasia, Schmid Type,Robin Sequence With Cleft Mandible And Limb Anomalies,Dysostosis,Vaginal Cancer,Neurodegeneration With Brain Iron Accumulation,Thrombocytopenia-Absent Radius Syndrome,Mandibulofacial Dysostosis, Guion-Almeida Type,Acrofacial Dysostosis |
6qdv_7 | P38919 | ENSG00000141543 | EIF4A3 | 99.40 | 8.80E-18 | 1.10E-21 | 183.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | Ifih1 |
Interferon-induced helicase C domain-containing protein 1 (EC 3.6.4.13) (Helicase with 2 CARD domains) (Helicard) (Interferon induced with helicase C domain protein 1) (Melanoma differentiation-associated protein 5) (MDA-5) (RIG-I-like receptor 2) (RLR-2) |
3.6.4.13 | Mus musculus | 6g19_a | Q8R5F7 | 99.40 | 3.20E-17 | 3.50E-21 | 200.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | GCN5 ADA4 SWI9 YGR252W |
Histone acetyltransferase GCN5 (EC 2.3.1.48) |
2.3.1.48 | Saccharomyces cerevisiae | 1e6i_a | Q03330 | 99.30 | 5.70E-16 | 5.10E-20 | 152.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | ERCC3 XPB XPBC |
General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (Basic transcription factor 2 89 kDa subunit) (BTF2 p89) (DNA excision repair protein ERCC-3) (DNA repair protein complementing XP-B cells) (TFIIH basal transcription factor complex 89 kDa subunit) (TFIIH 89 kDa subunit) (TFIIH p89) (Xeroderma pigmentosum group B-complementing protein) |
3.6.4.12 | Homo sapiens | Cerebro-Oculo-Facio-Skeletal Syndrome,Ichthyosis,Retinitis Pigmentosa,Hair Disease,Robinow Syndrome, Autosomal Recessive 1,Cockayne Syndrome A,Xeroderma Pigmentosum-Cockayne Syndrome Complex,Xeroderma Pigmentosum Group E,Trichothiodystrophy 1, Photosensitive,Cockayne Syndrome,Trichothiodystrophy,Breast Cancer,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group F,Xeroderma Pigmentosum, Complementation Group G,Skin Carcinoma,Xeroderma Pigmentosum, Complementation Group B,Xfe Progeroid Syndrome,Autosomal Recessive Disease,Trichothiodystrophy 2, Photosensitive,Trichothiodystrophy 3, Photosensitive,Ifap Syndrome 1, With Or Without Bresheck Syndrome,Uv-Sensitive Syndrome |
5of4_a | P19447 | ENSG00000163161 | ERCC3 | 99.50 | 1.50E-18 | 1.50E-22 | 210.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | SSL2 LOM3 RAD25 UVS112 YIL143C |
General transcription and DNA repair factor IIH helicase subunit XPB (TFIIH subunit XPB) (EC 3.6.4.12) (DNA repair helicase RAD25) (RNA polymerase II transcription factor B subunit SSL2) (TFB subunit SSL2) (Suppressor of stem-loop mutation 2) |
3.6.4.12 | Saccharomyces cerevisiae | 5fmf_1 | Q00578 | 99.30 | 6.90E-17 | 7.60E-21 | 189.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | DR_1289 |
DR_1289 |
3.6.4.12 | Deinococcus radiodurans | 4q47_a | Q9RUU2 | 99.40 | 1.80E-17 | 2.00E-21 | 196.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | CTHT_0054430 |
CTHT_0054430 |
Chaetomium thermophilum | 5dtu_a | G0SBQ7 | 99.20 | 1.40E-15 | 1.70E-19 | 172.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | rgy topR TM_0173 |
Reverse gyrase [Includes: Helicase (EC 3.6.4.12); Topoisomerase (EC 5.6.2.2)] |
5.6.2.2 | Thermotoga maritima | 3p4x_b | O51934 | 99.20 | 6.00E-16 | 6.50E-20 | 176.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | CHD1 YER164W SYGP-ORF4 |
Chromo domain-containing protein 1 (EC 3.6.4.-) (ATP-dependent helicase CHD1) |
3.6.4.- | Saccharomyces cerevisiae | 6ftx_w | P32657 | 99.80 | 3.10E-25 | 3.20E-29 | 283.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | Ddx58 |
Antiviral innate immune response receptor RIG-I (DEAD box protein 58) (Probable ATP-dependent RNA helicase DDX58) (EC 3.6.4.13) (RIG-I-like receptor 1) (RLR-1) (Retinoic acid-inducible gene 1 protein) (RIG-1) (Retinoic acid-inducible gene I protein) (RIG-I) |
3.6.4.13 | Mus musculus | 3tbk_a | Q6Q899 | 99.50 | 2.50E-18 | 2.90E-22 | 201.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | recQ b3822 JW5855 |
ATP-dependent DNA helicase RecQ (EC 3.6.4.12) |
3.6.4.12 | Escherichia coli | 1oyw_a | P15043 | 99.40 | 5.20E-18 | 5.80E-22 | 200.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YOR290C | SNF2 | SGDID:S000005816 | BLM RECQ2 RECQL3 |
Bloom syndrome protein (EC 3.6.4.12) (DNA helicase, RecQ-like type 2) (RecQ2) (RecQ protein-like 3) |
3.6.4.12 | Homo sapiens | Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Familial Colorectal Cancer,Inherited Cancer-Predisposing Syndrome,Wilms Tumor Predisposition,Ovarian Cancer,Breast Cancer,Hereditary Breast Ovarian Cancer Syndrome,Colorectal Cancer,Microcephaly,Werner Syndrome,Fanconi Anemia, Complementation Group A,Cone-Rod Dystrophy 2,Tumor Predisposition Syndrome,Syndromic Intellectual Disability,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Nijmegen Breakage Syndrome,Ataxia-Telangiectasia,Bloom Syndrome,Rapadilino Syndrome |
4o3m_a | P54132 | ENSG00000197299 | BLM | 99.20 | 6.90E-16 | 7.30E-20 | 188.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | SSO1653 |
SSO1653 |
Saccharolobus solfataricus | 1z63_b | Q97XQ7 | 99.70 | 2.90E-23 | 3.30E-27 | 242.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | MDA5 |
MDA5 |
3.6.4.13 | Gallus gallus | 5jcf_b | D9N195 | 99.40 | 2.20E-17 | 2.40E-21 | 202.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | DDX6 HLR2 RCK |
Probable ATP-dependent RNA helicase DDX6 (EC 3.6.4.13) (ATP-dependent RNA helicase p54) (DEAD box protein 6) (Oncogene RCK) |
3.6.4.13 | Homo sapiens | Nodal Marginal Zone Lymphoma,Non-Specific Syndromic Intellectual Disability,Noonan Syndrome 3,Telecanthus,Intellectual Developmental Disorder With Impaired Language And Dysmorphic Facies |
4ct4_b | P26196 | ENSG00000110367 | DDX6 | 99.40 | 3.60E-17 | 4.30E-21 | 178.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | MJ0669 |
Probable ATP-dependent RNA helicase MJ0669 (EC 3.6.4.13) |
3.6.4.13 | Methanocaldococcus jannaschii | 1hv8_a | Q58083 | 99.30 | 7.50E-17 | 9.10E-21 | 173.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | BmVLG |
BmVLG |
3.6.4.13 | Bombyx mori | 4d25_a | O01378 | 99.30 | 7.10E-17 | 8.30E-21 | 180.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | TIF1 TIF41A YKR059W; TIF2 TIF41B YJL138C J0660 |
ATP-dependent RNA helicase eIF4A (EC 3.6.4.13) (Eukaryotic initiation factor 4A) (eIF-4A) (Stimulator factor I 37 kDa component) (Translation initiation factor 1/2) (p37) |
3.6.4.13 | Saccharomyces cerevisiae | 1fuu_b | P10081 | 99.30 | 6.80E-17 | 8.00E-21 | 178.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | RECQL RECQ1 RECQL1 |
ATP-dependent DNA helicase Q1 (EC 3.6.4.12) (DNA helicase, RecQ-like type 1) (RecQ1) (DNA-dependent ATPase Q1) (RecQ protein-like 1) |
3.6.4.12 | Homo sapiens | Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Inherited Cancer-Predisposing Syndrome,Ovarian Cancer,Hereditary Breast Ovarian Cancer Syndrome,Werner Syndrome,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Tumor Predisposition Syndrome,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Bloom Syndrome,Rapadilino Syndrome |
2v1x_b | P46063 | ENSG00000004700 | RECQL | 99.40 | 1.80E-17 | 1.80E-21 | 202.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | ST2459 STK_24590 |
ST2459 STK_24590 |
3.6.4.13 | Sulfurisphaera tokodaii | 2z0m_a | Q96XQ7 | 99.20 | 1.50E-15 | 1.90E-19 | 160.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | rapA ECS88_0062 |
RNA polymerase-associated protein RapA (EC 3.6.4.-) (ATP-dependent helicase HepA) |
3.6.4.- | Escherichia coli | 6bog_b | B7MAI2 | 99.50 | 3.60E-19 | 3.50E-23 | 229.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | |||
YOR290C | SNF2 | SGDID:S000005816 | SNF2 GAM1 RIC1 SWI2 TYE3 YOR290C |
Transcription regulatory protein SNF2 (EC 3.6.4.-) (ATP-dependent helicase SNF2) (Regulatory protein GAM1) (Regulatory protein SWI2) (SWI/SNF complex component SNF2) (Transcription factor TYE3) |
3.6.4.- | Saccharomyces cerevisiae | 4i6m_c | P22082 | 99.70 | 2.90E-22 | 2.30E-26 | 195.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | DHX36 |
ATP-dependent DNA/RNA helicase DHX36 (EC 3.6.4.12) (EC 3.6.4.13) (DEAD/H box polypeptide 36) (DEAH-box protein 36) (G4-resolvase-1) (G4R1) (MLE-like protein 1) (RNA helicase associated with AU-rich element protein) |
3.6.4.13 | Bos taurus | 5vhe_a | Q05B79 | 99.30 | 1.20E-16 | 1.20E-20 | 204.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | MYCTH_2307364 |
MYCTH_2307364 |
Myceliophthora thermophila | 5jxr_a | G2QFM3 | 99.90 | 9.50E-31 | 9.30E-35 | 329.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | RECQL5 RECQ5 |
ATP-dependent DNA helicase Q5 (EC 3.6.4.12) (DNA helicase, RecQ-like type 5) (RecQ5) (RecQ protein-like 5) |
3.6.4.12 | Homo sapiens | Rothmund-Thomson Syndrome, Type 2,Baller-Gerold Syndrome,Werner Syndrome,Fanconi Anemia, Complementation Group A,Bloom Syndrome,Rapadilino Syndrome |
5lb3_e | O94762 | ENSG00000108469 | RECQL5 | 99.30 | 3.50E-16 | 4.00E-20 | 177.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | DHH1 YDL160C |
ATP-dependent RNA helicase DHH1 (EC 3.6.4.13) (DExD/H-box helicase 1) |
3.6.4.13 | Saccharomyces cerevisiae | 1s2m_a | P39517 | 99.40 | 4.80E-17 | 5.70E-21 | 179.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | Rhau 38E.15 cg9323 DmDHX36 Dmel\CG9323 DmRHAU RHAU CG9323 Dmel_CG9323 |
Rhau 38E.15 cg9323 DmDHX36 Dmel\CG9323 DmRHAU RHAU CG9323 Dmel_CG9323 |
3.6.4.12,3.6.4.13, | Drosophila melanogaster | 5n8r_b | Q8SWT2 | 99.20 | 1.00E-15 | 1.10E-19 | 195.40 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | cshA GT50_10605 |
cshA GT50_10605 |
Geobacillus stearothermophilus | 5ivl_b | A0A0K2H973 | 99.40 | 1.00E-17 | 1.20E-21 | 188.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | DBP5 RAT8 YOR046C |
ATP-dependent RNA helicase DBP5 (EC 3.6.4.13) (DEAD box protein 5) (Helicase CA5/6) (Ribonucleic acid-trafficking protein 8) |
3.6.4.13 | Saccharomyces cerevisiae | 3pey_a | P20449 | 99.20 | 7.40E-16 | 8.90E-20 | 168.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | HAS1 YMR290C |
ATP-dependent RNA helicase HAS1 (EC 3.6.4.13) (Helicase associated with SET1 protein 1) |
3.6.4.13 | Saccharomyces cerevisiae | 5z3g_y | Q03532 | 99.40 | 9.70E-18 | 1.10E-21 | 196.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | DDX19B DBP5 DDX19 TDBP |
ATP-dependent RNA helicase DDX19B (EC 3.6.4.13) (DEAD box RNA helicase DEAD5) (DEAD box protein 19B) |
3.6.4.13 | Homo sapiens | Anterior Horn Cell Disease,Lethal Congenital Contracture Syndrome 1,Lethal Congenital Contracture Syndrome |
6b4j_e | Q9UMR2 | ENSG00000157349 | DDX19B | 99.30 | 2.10E-16 | 2.50E-20 | 178.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | RNA helicase (EC 3.6.4.13) |
RNA helicase (EC 3.6.4.13) |
3.6.4.13 | Gallus gallus | 5jaj_a | G0YYQ5 | 99.50 | 1.30E-18 | 1.40E-22 | 212.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | hel308 hjm PF0677 |
ATP-dependent DNA helicase Hel308 (EC 3.6.4.12) (ATP-dependent Holliday junction unwindase Hjm) (Holliday junction migration DNA helicase) |
3.6.4.12 | Pyrococcus furiosus | 2zj8_a | O73946 | 99.20 | 8.00E-16 | 8.70E-20 | 188.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | SKI2 YLR398C L8084.17 |
Antiviral helicase SKI2 (EC 3.6.4.13) (Superkiller protein 2) |
3.6.4.13 | Saccharomyces cerevisiae | 4buj_a | P35207 | 99.40 | 2.10E-17 | 2.10E-21 | 214.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | DNA repair and recombination protein RAD54-like (EC 3.6.4.12) |
Danio rerio | 1z3i_x | Q7ZV09 | 99.80 | 3.20E-25 | 3.50E-29 | 268.90 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | |||||
YOR290C | SNF2 | SGDID:S000005816 | MSS116 YDR194C YD9346.05C |
ATP-dependent RNA helicase MSS116, mitochondrial (EC 3.6.4.13) |
3.6.4.13 | Saccharomyces cerevisiae | 3i5x_a | P15424 | 99.30 | 1.40E-16 | 1.60E-20 | 189.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | EIF4A1 DDX2A EIF4A |
Eukaryotic initiation factor 4A-I (eIF-4A-I) (eIF4A-I) (EC 3.6.4.13) (ATP-dependent RNA helicase eIF4A-1) |
3.6.4.13 | Homo sapiens | Ovary Sarcoma |
5zc9_a | P60842 | ENSG00000161960 | EIF4A1 | 99.40 | 2.90E-17 | 3.40E-21 | 180.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | DDX23 |
Probable ATP-dependent RNA helicase DDX23 (EC 3.6.4.13) (100 kDa U5 snRNP-specific protein) (DEAD box protein 23) (PRP28 homolog) (U5-100kD) |
3.6.4.13 | Homo sapiens | Retinitis Pigmentosa,Burn-Mckeown Syndrome,Distal Hereditary Motor Neuronopathy Type 2,Cockayne Syndrome,Spinal Muscular Atrophy, Type I |
4nho_a | Q9BUQ8 | ENSG00000174243 | DDX23 | 99.30 | 3.40E-16 | 3.90E-20 | 179.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOR290C | SNF2 | SGDID:S000005816 | CTHT_0026210 |
CTHT_0026210 |
Chaetomium thermophilum | 6g7e_b | G0S6C0 | 99.70 | 5.20E-23 | 5.60E-27 | 279.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | AF_0358 |
AF_0358 |
3.6.4.12 | Archaeoglobus fulgidus | 2fwr_a | O29889 | 99.40 | 4.70E-18 | 5.10E-22 | 197.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | secA div+ BSU35300 |
Protein translocase subunit SecA |
Bacillus subtilis | 1tf5_a | P28366 | 99.30 | 2.20E-16 | 2.40E-20 | 197.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | Autoprotease p20 (EC 2.7.7.48) (EC 3.4.21.113) (EC 3.6.1.15) (EC 3.6.4.13) (Capsid protein C) (Cysteine protease NS2) (E(rns) glycoprotein) (Envelope glycoprotein E1) (Envelope glycoprotein E2) (Genome polyprotein) (N-terminal protease) (NS5B) (Non-structural protein 2) (Non-structural protein 2-3) (Non-structural protein 3) (Non-structural protein 4A) (Non-structural protein 4B) (Non-structural protein 5A) (RNA-directed RNA polymerase) (Serine protease NS3) (Viroporin p7) (gp33) (gp44/48) (gp55) |
Autoprotease p20 (EC 2.7.7.48) (EC 3.4.21.113) (EC 3.6.1.15) (EC 3.6.4.13) (Capsid protein C) (Cysteine protease NS2) (E(rns) glycoprotein) (Envelope glycoprotein E1) (Envelope glycoprotein E2) (Genome polyprotein) (N-terminal protease) (NS5B) (Non-structural protein 2) (Non-structural protein 2-3) (Non-structural protein 3) (Non-structural protein 4A) (Non-structural protein 4B) (Non-structural protein 5A) (RNA-directed RNA polymerase) (Serine protease NS3) (Viroporin p7) (gp33) (gp44/48) (gp55) |
2.7.7.48,3.4.21.113,3.6.1.15,3.6.4.13, | Classical swine | 5wx1_a | Q5U8X5 | 99.20 | 8.60E-16 | 8.60E-20 | 192.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | secA azi pea prlD b0098 JW0096 |
Protein translocase subunit SecA |
Escherichia coli | 2fsh_b | P10408 | 99.20 | 1.90E-15 | 1.90E-19 | 191.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | ||||
YOR290C | SNF2 | SGDID:S000005816 | MTR4 DOB1 YJL050W J1158 |
ATP-dependent RNA helicase DOB1 (EC 3.6.4.13) (mRNA transport regulator MTR4) |
3.6.4.13 | Saccharomyces cerevisiae | 4u4c_a | P47047 | 99.20 | 7.40E-16 | 7.70E-20 | 197.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | xpb2 ST1613 STK_16130 |
xpb2 ST1613 STK_16130 |
Sulfurisphaera tokodaii | 5tnu_a | Q970I2 | 99.40 | 1.60E-17 | 1.80E-21 | 191.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YOR290C | SNF2 | SGDID:S000005816 | RIG-I |
RIG-I |
3.6.4.13 | Anas platyrhynchos | 4a36_a | D3TI84 | 99.40 | 2.50E-17 | 2.90E-21 | 192.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | PRP28 YDR243C YD8419.10C |
Pre-mRNA-splicing ATP-dependent RNA helicase PRP28 (EC 3.6.4.13) (Helicase CA8) |
3.6.4.13 | Saccharomyces cerevisiae | 4w7s_a | P23394 | 99.40 | 4.30E-17 | 5.00E-21 | 185.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | SUB2 YDL084W |
ATP-dependent RNA helicase SUB2 (EC 3.6.4.13) (Suppressor of BRR1 protein 2) |
3.6.4.13 | Saccharomyces cerevisiae | 5sup_b | Q07478 | 99.40 | 2.00E-17 | 2.40E-21 | 181.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOR290C | SNF2 | SGDID:S000005816 | DDX3X DBX DDX3 |
ATP-dependent RNA helicase DDX3X (EC 3.6.4.13) (CAP-Rf) (DEAD box protein 3, X-chromosomal) (DEAD box, X isoform) (DBX) (Helicase-like protein 2) (HLP2) |
3.6.4.13 | Homo sapiens | Hepatitis C,Hepatitis B,Venezuelan Equine Encephalitis,Encephalitis,Corpus Callosum, Agenesis Of, With Facial Anomalies And Robin Sequence,Lymphocytic Choriomeningitis,Rare Genetic Intellectual Disability,Hepatitis,Infratentorial Cancer,Ddx3x-Related Neurodevelopmental Disorder,Basal Cell Nevus Syndrome,Precursor T-Cell Acute Lymphoblastic Leukemia,Breast Cancer,Microcephaly,Hepatitis C Virus,Alacrima, Achalasia, And Mental Retardation Syndrome,Noonan Syndrome 3,Disease Of Mental Health,Adult Medulloblastoma,Childhood Medulloblastoma,Intellectual Developmental Disorder, X-Linked, Syndromic, Snijders Blok Type,Ewing Sarcoma,Syndromic Intellectual Disability,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Medulloblastoma,Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma Of Childhood,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay |
2i4i_a | O00571 | ENSG00000215301 | DDX3X | 99.30 | 1.50E-16 | 1.80E-20 | 175.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |