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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
Related structures:
AlphaFold database: A4HKM9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006833 | water transport | 5 | 1 |
GO:0042044 | fluid transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 20 |
GO:0015267 | channel activity | 4 | 20 |
GO:0022803 | passive transmembrane transporter activity | 3 | 20 |
GO:0022857 | transmembrane transporter activity | 2 | 20 |
GO:0005372 | water transmembrane transporter activity | 4 | 1 |
GO:0015250 | water channel activity | 5 | 1 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.629 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.468 |
CLV_Separin_Metazoa | 386 | 390 | PF03568 | 0.604 |
DEG_ODPH_VHL_1 | 287 | 300 | PF01847 | 0.345 |
DOC_MAPK_MEF2A_6 | 31 | 38 | PF00069 | 0.558 |
DOC_PP2B_LxvP_1 | 75 | 78 | PF13499 | 0.519 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.563 |
LIG_14-3-3_CanoR_1 | 366 | 372 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 66 | 75 | PF00244 | 0.504 |
LIG_Actin_WH2_2 | 265 | 282 | PF00022 | 0.290 |
LIG_AP2alpha_2 | 50 | 52 | PF02296 | 0.530 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.422 |
LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.211 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.411 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.314 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.474 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.596 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.561 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.544 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.621 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.611 |
LIG_GBD_Chelix_1 | 290 | 298 | PF00786 | 0.350 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 70 | 78 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 79 | 87 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 79 | 83 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.420 |
LIG_MAD2 | 20 | 28 | PF02301 | 0.590 |
LIG_NRBOX | 294 | 300 | PF00104 | 0.218 |
LIG_PDZ_Class_3 | 399 | 404 | PF00595 | 0.587 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.279 |
LIG_PTB_Apo_2 | 220 | 227 | PF02174 | 0.234 |
LIG_PTB_Apo_2 | 3 | 10 | PF02174 | 0.562 |
LIG_PTB_Phospho_1 | 220 | 226 | PF10480 | 0.234 |
LIG_SH2_CRK | 72 | 76 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.617 |
LIG_SH2_STAT3 | 226 | 229 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.296 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.712 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.183 |
LIG_SUMO_SIM_par_1 | 102 | 108 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.263 |
LIG_TRAF2_1 | 395 | 398 | PF00917 | 0.618 |
LIG_TRFH_1 | 285 | 289 | PF08558 | 0.345 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.297 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.287 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.323 |
LIG_WW_3 | 386 | 390 | PF00397 | 0.647 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.265 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.561 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.430 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.222 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.717 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.800 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.610 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.617 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.613 |
MOD_CMANNOS | 283 | 286 | PF00535 | 0.316 |
MOD_Cter_Amidation | 188 | 191 | PF01082 | 0.367 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.315 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.449 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.287 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.209 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.352 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.494 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.538 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.501 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.502 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.394 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.271 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.586 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.364 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.193 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.679 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.662 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.710 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.591 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.411 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.411 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.309 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.389 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.297 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.399 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.368 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.620 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.597 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.604 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.447 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.346 |
MOD_NEK2_2 | 105 | 110 | PF00069 | 0.345 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.339 |
MOD_PIKK_1 | 306 | 312 | PF00454 | 0.564 |
MOD_PK_1 | 110 | 116 | PF00069 | 0.225 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.771 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.411 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.584 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.600 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.211 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.211 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.588 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.248 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.403 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.256 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.518 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.503 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.452 |
MOD_SUMO_rev_2 | 308 | 317 | PF00179 | 0.641 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.622 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.617 |
TRG_Pf-PMV_PEXEL_1 | 389 | 394 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I348 | Leptomonas seymouri | 66% | 67% |
A0A0S4JRP5 | Bodo saltans | 26% | 100% |
A0A1X0NRT6 | Trypanosomatidae | 61% | 90% |
A0A3Q8IFK5 | Leishmania donovani | 76% | 68% |
A0A3S5H7B2 | Leishmania donovani | 36% | 100% |
A0A3S5H7S4 | Leishmania donovani | 36% | 100% |
A0A422N886 | Trypanosoma rangeli | 57% | 96% |
A4HCI0 | Leishmania braziliensis | 32% | 97% |
A4HKM8 | Leishmania braziliensis | 38% | 100% |
A4I001 | Leishmania infantum | 36% | 100% |
A4I858 | Leishmania infantum | 76% | 68% |
A4I859 | Leishmania infantum | 36% | 100% |
E9AVX4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B316 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B317 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 68% |
G5CTG4 | Milnesium tardigradum | 25% | 100% |
Q4Q537 | Leishmania major | 76% | 100% |
Q4Q538 | Leishmania major | 37% | 100% |
Q4QBK5 | Leishmania major | 37% | 100% |
Q54WT8 | Dictyostelium discoideum | 26% | 100% |
V5D449 | Trypanosoma cruzi | 63% | 90% |