by homology
Contact email: antonio.jimenez@uah.es
Publication title: A functional BH3 domain in an aquaporin from Leishmania infantum
Publication 1st author(s): Genes
Publication Identifier(s): 27551533
Host organism: taxid:4932
Interaction detection method(s): two hybrid
Interaction type: physical association
Identification method participant A: predetermined participant
Identification method participant B: predetermined participant
ID(s) interactor A: Q07817
ID(s) interactor B: A4I001
Taxid interactor A: Homo sapiens
Taxid interactor B: Leishmania infantum
Biological role(s) interactor A: unspecified role
Biological role(s) interactor B: unspecified role
Experimental role(s) interactor A: bait
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 0 |
| Forrest at al. (procyclic) | no | yes: 0 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 32 |
| NetGPI | no | yes: 0, no: 32 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 33 |
| GO:0110165 | cellular anatomical entity | 1 | 33 |
| GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4HCI0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 2 |
| GO:0006833 | water transport | 5 | 2 |
| GO:0042044 | fluid transport | 4 | 2 |
| GO:0051179 | localization | 1 | 2 |
| GO:0051234 | establishment of localization | 2 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 33 |
| GO:0015267 | channel activity | 4 | 33 |
| GO:0022803 | passive transmembrane transporter activity | 3 | 33 |
| GO:0022857 | transmembrane transporter activity | 2 | 33 |
| GO:0005372 | water transmembrane transporter activity | 4 | 2 |
| GO:0015250 | water channel activity | 5 | 2 |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.263 |
| CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.332 |
| CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.298 |
| CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.474 |
| CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.450 |
| CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.525 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.566 |
| DOC_CKS1_1 | 242 | 247 | PF01111 | 0.404 |
| DOC_CYCLIN_RxL_1 | 247 | 256 | PF00134 | 0.211 |
| DOC_MAPK_gen_1 | 143 | 149 | PF00069 | 0.484 |
| DOC_PP4_FxxP_1 | 171 | 174 | PF00568 | 0.262 |
| DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.238 |
| DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.449 |
| DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.404 |
| LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.407 |
| LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.249 |
| LIG_14-3-3_CanoR_1 | 30 | 40 | PF00244 | 0.699 |
| LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.305 |
| LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.623 |
| LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.321 |
| LIG_EH1_1 | 139 | 147 | PF00400 | 0.395 |
| LIG_FHA_1 | 122 | 128 | PF00498 | 0.344 |
| LIG_FHA_1 | 192 | 198 | PF00498 | 0.275 |
| LIG_FHA_1 | 241 | 247 | PF00498 | 0.299 |
| LIG_FHA_1 | 32 | 38 | PF00498 | 0.704 |
| LIG_FHA_1 | 76 | 82 | PF00498 | 0.285 |
| LIG_GBD_Chelix_1 | 158 | 166 | PF00786 | 0.187 |
| LIG_GBD_Chelix_1 | 72 | 80 | PF00786 | 0.279 |
| LIG_Integrin_isoDGR_2 | 167 | 169 | PF01839 | 0.520 |
| LIG_LIR_Apic_2 | 170 | 174 | PF02991 | 0.261 |
| LIG_LIR_Gen_1 | 190 | 201 | PF02991 | 0.312 |
| LIG_LIR_Gen_1 | 281 | 290 | PF02991 | 0.378 |
| LIG_LIR_Gen_1 | 61 | 72 | PF02991 | 0.499 |
| LIG_LIR_Gen_1 | 78 | 87 | PF02991 | 0.247 |
| LIG_LIR_Gen_1 | 99 | 109 | PF02991 | 0.337 |
| LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.282 |
| LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.275 |
| LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.257 |
| LIG_LIR_Nem_3 | 213 | 217 | PF02991 | 0.359 |
| LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.294 |
| LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.519 |
| LIG_LIR_Nem_3 | 78 | 82 | PF02991 | 0.252 |
| LIG_PDZ_Class_3 | 289 | 294 | PF00595 | 0.584 |
| LIG_Pex14_2 | 217 | 221 | PF04695 | 0.383 |
| LIG_Pex14_2 | 75 | 79 | PF04695 | 0.297 |
| LIG_SH2_PTP2 | 284 | 287 | PF00017 | 0.391 |
| LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.447 |
| LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.297 |
| LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.525 |
| LIG_SH3_3 | 234 | 240 | PF00018 | 0.404 |
| LIG_SH3_3 | 7 | 13 | PF00018 | 0.730 |
| LIG_SUMO_SIM_anti_2 | 243 | 250 | PF11976 | 0.299 |
| LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.304 |
| LIG_SUMO_SIM_par_1 | 121 | 126 | PF11976 | 0.382 |
| LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.291 |
| LIG_TYR_ITIM | 282 | 287 | PF00017 | 0.308 |
| LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.240 |
| LIG_WRC_WIRS_1 | 192 | 197 | PF05994 | 0.278 |
| LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.277 |
| MOD_CK1_1 | 179 | 185 | PF00069 | 0.197 |
| MOD_CK1_1 | 191 | 197 | PF00069 | 0.257 |
| MOD_CK1_1 | 258 | 264 | PF00069 | 0.192 |
| MOD_CK1_1 | 86 | 92 | PF00069 | 0.308 |
| MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.234 |
| MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.512 |
| MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.444 |
| MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.406 |
| MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.394 |
| MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.206 |
| MOD_GSK3_1 | 103 | 110 | PF00069 | 0.304 |
| MOD_GSK3_1 | 251 | 258 | PF00069 | 0.180 |
| MOD_GSK3_1 | 54 | 61 | PF00069 | 0.613 |
| MOD_GSK3_1 | 81 | 88 | PF00069 | 0.282 |
| MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.476 |
| MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.242 |
| MOD_NEK2_1 | 103 | 108 | PF00069 | 0.261 |
| MOD_NEK2_1 | 129 | 134 | PF00069 | 0.464 |
| MOD_NEK2_1 | 176 | 181 | PF00069 | 0.267 |
| MOD_NEK2_1 | 188 | 193 | PF00069 | 0.251 |
| MOD_NEK2_1 | 253 | 258 | PF00069 | 0.235 |
| MOD_NEK2_1 | 278 | 283 | PF00069 | 0.271 |
| MOD_NEK2_1 | 75 | 80 | PF00069 | 0.284 |
| MOD_NEK2_1 | 81 | 86 | PF00069 | 0.289 |
| MOD_NEK2_2 | 138 | 143 | PF00069 | 0.429 |
| MOD_NEK2_2 | 58 | 63 | PF00069 | 0.655 |
| MOD_OFUCOSY | 225 | 230 | PF10250 | 0.211 |
| MOD_PIKK_1 | 204 | 210 | PF00454 | 0.526 |
| MOD_PKA_1 | 54 | 60 | PF00069 | 0.496 |
| MOD_PKA_2 | 4 | 10 | PF00069 | 0.688 |
| MOD_Plk_1 | 20 | 26 | PF00069 | 0.538 |
| MOD_Plk_1 | 210 | 216 | PF00069 | 0.340 |
| MOD_Plk_4 | 103 | 109 | PF00069 | 0.279 |
| MOD_Plk_4 | 179 | 185 | PF00069 | 0.213 |
| MOD_Plk_4 | 188 | 194 | PF00069 | 0.277 |
| MOD_Plk_4 | 196 | 202 | PF00069 | 0.275 |
| MOD_Plk_4 | 210 | 216 | PF00069 | 0.445 |
| MOD_Plk_4 | 262 | 268 | PF00069 | 0.244 |
| MOD_Plk_4 | 278 | 284 | PF00069 | 0.252 |
| MOD_Plk_4 | 75 | 81 | PF00069 | 0.283 |
| MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.404 |
| TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.525 |
| TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.450 |
| TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.518 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1D2 | Leptomonas seymouri | 68% | 100% |
| A0A0N1ILB4 | Leptomonas seymouri | 38% | 100% |
| A0A0N1PB10 | Leptomonas seymouri | 39% | 100% |
| A0A0S4IS36 | Bodo saltans | 32% | 84% |
| A0A0S4IS78 | Bodo saltans | 38% | 100% |
| A0A0S4JRP5 | Bodo saltans | 25% | 88% |
| A0A0S4KLV5 | Bodo saltans | 38% | 100% |
| A0A1X0ND19 | Trypanosomatidae | 39% | 100% |
| A0A1X0NT73 | Trypanosomatidae | 36% | 100% |
| A0A1X0NTY8 | Trypanosomatidae | 55% | 100% |
| A0A3R7RFH0 | Trypanosoma rangeli | 37% | 100% |
| A0A3S5H7B2 | Leishmania donovani | 77% | 100% |
| A0A3S5H7S4 | Leishmania donovani | 37% | 100% |
| A0A3S7X8F2 | Leishmania donovani | 38% | 100% |
| A0A422N493 | Trypanosoma rangeli | 58% | 100% |
| A0A422N886 | Trypanosoma rangeli | 36% | 70% |
| A0A422NSX8 | Trypanosoma rangeli | 38% | 100% |
| A0A6M3QG69 | Musa acuminata | 25% | 100% |
| A0A804KTT0 | Musa acuminata subsp. malaccensis | 26% | 100% |
| A4HBA6 | Leishmania braziliensis | 39% | 100% |
| A4HKM8 | Leishmania braziliensis | 37% | 100% |
| A4HKM9 | Leishmania braziliensis | 32% | 73% |
| A4I001 | Leishmania infantum | 77% | 100% |
| A4I859 | Leishmania infantum | 37% | 100% |
| A4IAF4 | Leishmania infantum | 38% | 100% |
| A4L9J0 | Oryctolagus cuniculus | 30% | 100% |
| A8W649 | Sus scrofa | 29% | 100% |
| E9AVX4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
| E9B316 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
| E9B5H8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
| F9UUD2 | Lactiplantibacillus plantarum (strain ATCC BAA-793 / NCIMB 8826 / WCFS1) | 26% | 100% |
| O26206 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 27% | 100% |
| O62735 | Ovis aries | 26% | 100% |
| O77750 | Bos taurus | 28% | 91% |
| O82316 | Arabidopsis thaliana | 27% | 100% |
| O86231 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 26% | 100% |
| P06624 | Bos taurus | 30% | 100% |
| P08995 | Glycine max | 28% | 100% |
| P09011 | Rattus norvegicus | 28% | 100% |
| P0DO54 | Musa acuminata | 25% | 100% |
| P25794 | Pisum sativum | 28% | 100% |
| P25818 | Arabidopsis thaliana | 27% | 100% |
| P29972 | Homo sapiens | 26% | 100% |
| P29975 | Rattus norvegicus | 26% | 100% |
| P34080 | Rattus norvegicus | 26% | 100% |
| P42067 | Medicago sativa | 26% | 100% |
| P42767 | Atriplex canescens | 27% | 100% |
| P47863 | Rattus norvegicus | 29% | 91% |
| P47864 | Rattus norvegicus | 29% | 100% |
| P47865 | Bos taurus | 29% | 100% |
| P49173 | Nicotiana alata | 25% | 100% |
| P50501 | Pelophylax lessonae | 28% | 100% |
| P51180 | Mus musculus | 28% | 100% |
| P55064 | Homo sapiens | 28% | 100% |
| P55087 | Homo sapiens | 29% | 91% |
| P55088 | Mus musculus | 29% | 91% |
| P56401 | Ovis aries | 28% | 100% |
| P56402 | Mus musculus | 26% | 100% |
| P61837 | Arabidopsis thaliana | 28% | 100% |
| P61838 | Vicia faba | 28% | 100% |
| P73809 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 28% | 100% |
| P79099 | Bos taurus | 27% | 100% |
| P93004 | Arabidopsis thaliana | 27% | 100% |
| Q02013 | Mus musculus | 27% | 100% |
| Q06019 | Lithobates pipiens | 30% | 100% |
| Q06611 | Arabidopsis thaliana | 27% | 100% |
| Q08451 | Solanum lycopersicum | 28% | 100% |
| Q08733 | Arabidopsis thaliana | 27% | 100% |
| Q0IWF3 | Oryza sativa subsp. japonica | 27% | 95% |
| Q19KC1 | Zea mays | 23% | 100% |
| Q23808 | Cicadella viridis | 30% | 100% |
| Q25074 | Haematobia irritans exigua | 26% | 100% |
| Q39196 | Arabidopsis thaliana | 27% | 100% |
| Q41963 | Arabidopsis thaliana | 29% | 100% |
| Q4Q2F7 | Leishmania major | 38% | 100% |
| Q4Q538 | Leishmania major | 36% | 100% |
| Q4QBK5 | Leishmania major | 75% | 100% |
| Q54WT8 | Dictyostelium discoideum | 27% | 100% |
| Q5I4F9 | Notomys alexis | 29% | 90% |
| Q5R819 | Pongo abelii | 27% | 100% |
| Q5Z6F0 | Oryza sativa subsp. japonica | 27% | 100% |
| Q651D5 | Oryza sativa subsp. japonica | 28% | 100% |
| Q67WJ8 | Oryza sativa subsp. japonica | 25% | 99% |
| Q6EU94 | Oryza sativa subsp. japonica | 27% | 100% |
| Q6J8I9 | Ovis aries | 30% | 100% |
| Q6K215 | Oryza sativa subsp. japonica | 27% | 100% |
| Q6PQZ1 | Sus scrofa | 28% | 100% |
| Q6Z2T3 | Oryza sativa subsp. japonica | 25% | 99% |
| Q7EYH7 | Oryza sativa subsp. japonica | 28% | 96% |
| Q7MIV9 | Vibrio vulnificus (strain YJ016) | 26% | 100% |
| Q7N5C1 | Photorhabdus laumondii subsp. laumondii (strain DSM 15139 / CIP 105565 / TT01) | 28% | 100% |
| Q7NNP3 | Gloeobacter violaceus (strain ATCC 29082 / PCC 7421) | 27% | 100% |
| Q7PWV1 | Anopheles gambiae | 31% | 100% |
| Q7XLR1 | Oryza sativa subsp. japonica | 27% | 100% |
| Q7XSQ9 | Oryza sativa subsp. japonica | 26% | 100% |
| Q7Y1E6 | Oryza sativa subsp. japonica | 30% | 100% |
| Q84RL6 | Zea mays | 27% | 100% |
| Q84S07 | Oryza sativa subsp. japonica | 25% | 100% |
| Q866S3 | Ovis aries | 27% | 100% |
| Q87MQ5 | Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) | 25% | 100% |
| Q88F17 | Pseudomonas putida (strain ATCC 47054 / DSM 6125 / CFBP 8728 / NCIMB 11950 / KT2440) | 26% | 100% |
| Q8DB17 | Vibrio vulnificus (strain CMCP6) | 25% | 100% |
| Q8EHC1 | Shewanella oneidensis (strain MR-1) | 26% | 100% |
| Q8FY85 | Brucella suis biovar 1 (strain 1330) | 27% | 100% |
| Q8H5N9 | Oryza sativa subsp. japonica | 27% | 100% |
| Q8LAA6 | Arabidopsis thaliana | 28% | 100% |
| Q8LAI1 | Arabidopsis thaliana | 26% | 100% |
| Q8LFP7 | Arabidopsis thaliana | 29% | 100% |
| Q8VZW1 | Arabidopsis thaliana | 29% | 99% |
| Q923J4 | Dipodomys merriami | 29% | 91% |
| Q9AQU5 | Zea mays | 27% | 100% |
| Q9AR14 | Zea mays | 27% | 100% |
| Q9AT74 | Zea mays | 25% | 98% |
| Q9ATL2 | Zea mays | 26% | 100% |
| Q9ATM4 | Zea mays | 26% | 100% |
| Q9ATN0 | Zea mays | 28% | 99% |
| Q9ATN1 | Zea mays | 26% | 97% |
| Q9ATN2 | Zea mays | 25% | 100% |
| Q9C4Z5 | Methanothermobacter marburgensis (strain ATCC BAA-927 / DSM 2133 / JCM 14651 / NBRC 100331 / OCM 82 / Marburg) | 26% | 100% |
| Q9C6T0 | Arabidopsis thaliana | 27% | 91% |
| Q9FIZ9 | Arabidopsis thaliana | 24% | 100% |
| Q9FY14 | Medicago truncatula | 26% | 100% |
| Q9HWZ3 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 27% | 100% |
| Q9N2J4 | Canis lupus familiaris | 27% | 100% |
| Q9NHW7 | Aedes aegypti | 29% | 100% |
| Q9SAI4 | Arabidopsis thaliana | 26% | 96% |
| Q9SV84 | Arabidopsis thaliana | 28% | 97% |
| Q9SXF8 | Oryza sativa subsp. japonica | 27% | 100% |
| Q9U8P7 | Dictyostelium discoideum | 26% | 100% |
| Q9V5Z7 | Drosophila melanogaster | 28% | 100% |
| Q9WTY4 | Mus musculus | 29% | 100% |
| Q9XF59 | Zea mays | 26% | 100% |
| Q9ZVX8 | Arabidopsis thaliana | 27% | 100% |
| S5ZH89 | Musa acuminata | 26% | 100% |
| V5ANF5 | Trypanosoma cruzi | 38% | 100% |
| V5B469 | Trypanosoma cruzi | 57% | 100% |
| V5BW46 | Trypanosoma cruzi | 37% | 100% |