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: 33 |
NetGPI | no | yes: 0, no: 33 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: A4HB01
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.578 |
CLV_C14_Caspase3-7 | 543 | 547 | PF00656 | 0.423 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.617 |
CLV_PCSK_FUR_1 | 494 | 498 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.461 |
DEG_APCC_DBOX_1 | 307 | 315 | PF00400 | 0.437 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.256 |
DEG_APCC_DBOX_1 | 525 | 533 | PF00400 | 0.376 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.626 |
DEG_SPOP_SBC_1 | 479 | 483 | PF00917 | 0.257 |
DOC_CYCLIN_RxL_1 | 212 | 222 | PF00134 | 0.619 |
DOC_CYCLIN_yCln2_LP_2 | 276 | 282 | PF00134 | 0.304 |
DOC_MAPK_DCC_7 | 342 | 350 | PF00069 | 0.355 |
DOC_MAPK_gen_1 | 173 | 182 | PF00069 | 0.549 |
DOC_MAPK_gen_1 | 389 | 399 | PF00069 | 0.257 |
DOC_MAPK_gen_1 | 410 | 420 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 265 | 273 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 342 | 350 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 392 | 400 | PF00069 | 0.344 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.266 |
DOC_PP4_FxxP_1 | 73 | 76 | PF00568 | 0.659 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.380 |
DOC_USP7_MATH_2 | 432 | 438 | PF00917 | 0.282 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 199 | 203 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 230 | 234 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 274 | 279 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 353 | 359 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 496 | 503 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 7 | 14 | PF00244 | 0.784 |
LIG_Actin_WH2_2 | 345 | 362 | PF00022 | 0.360 |
LIG_BRCT_BRCA1_1 | 571 | 575 | PF00533 | 0.287 |
LIG_CtBP_PxDLS_1 | 469 | 473 | PF00389 | 0.297 |
LIG_deltaCOP1_diTrp_1 | 566 | 575 | PF00928 | 0.326 |
LIG_eIF4E_1 | 503 | 509 | PF01652 | 0.309 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.561 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.515 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.307 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.293 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.381 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.499 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.598 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.599 |
LIG_LIR_Gen_1 | 473 | 479 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 144 | 148 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.283 |
LIG_PDZ_Wminus1_1 | 582 | 584 | PF00595 | 0.277 |
LIG_Pex14_2 | 251 | 255 | PF04695 | 0.298 |
LIG_REV1ctd_RIR_1 | 37 | 46 | PF16727 | 0.557 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.521 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.277 |
LIG_SH2_CRK | 561 | 565 | PF00017 | 0.382 |
LIG_SH2_GRB2like | 503 | 506 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.377 |
LIG_SH2_SRC | 561 | 564 | PF00017 | 0.406 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 260 | 263 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.548 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.388 |
LIG_SUMO_SIM_anti_2 | 394 | 401 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 128 | 134 | PF11976 | 0.574 |
LIG_SUMO_SIM_par_1 | 468 | 473 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 75 | 82 | PF11976 | 0.537 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.476 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.288 |
LIG_TYR_ITIM | 559 | 564 | PF00017 | 0.354 |
LIG_TYR_ITSM | 232 | 239 | PF00017 | 0.523 |
MOD_CDK_SPxxK_3 | 25 | 32 | PF00069 | 0.529 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.689 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.495 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.477 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.628 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.288 |
MOD_CK2_1 | 518 | 524 | PF00069 | 0.282 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.438 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.287 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.280 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.685 |
MOD_GlcNHglycan | 303 | 307 | PF01048 | 0.627 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.580 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.409 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.612 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.509 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.532 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.568 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.665 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.447 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.413 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.362 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.660 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.370 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.496 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.682 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.637 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.461 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.564 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.351 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.359 |
MOD_NEK2_1 | 550 | 555 | PF00069 | 0.271 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.301 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.345 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.295 |
MOD_PIKK_1 | 460 | 466 | PF00454 | 0.373 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.434 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.507 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.581 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.338 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.385 |
MOD_PKB_1 | 300 | 308 | PF00069 | 0.289 |
MOD_PKB_1 | 401 | 409 | PF00069 | 0.356 |
MOD_PKB_1 | 494 | 502 | PF00069 | 0.284 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.262 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.404 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.386 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.411 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.495 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.304 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.572 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.286 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.567 |
TRG_DiLeu_BaEn_1 | 394 | 399 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.295 |
TRG_DiLeu_BaLyEn_6 | 504 | 509 | PF01217 | 0.249 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 400 | 403 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 493 | 496 | PF00400 | 0.466 |
TRG_NES_CRM1_1 | 357 | 372 | PF08389 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 43% | 89% |
A0A0N1PB02 | Leptomonas seymouri | 68% | 89% |
A0A0S4J6C6 | Bodo saltans | 44% | 90% |
A0A1X0P9A6 | Trypanosomatidae | 53% | 86% |
A0A3Q8IHH1 | Leishmania donovani | 41% | 80% |
A0A3R7K2Y9 | Trypanosoma rangeli | 52% | 85% |
A0A3S5H668 | Leishmania donovani | 47% | 100% |
A0A3S5H669 | Leishmania donovani | 46% | 92% |
A0A3S7X835 | Leishmania donovani | 70% | 100% |
A4H5C9 | Leishmania braziliensis | 48% | 100% |
A4H5D0 | Leishmania braziliensis | 47% | 100% |
A4HAZ7 | Leishmania braziliensis | 94% | 100% |
A4HAZ9 | Leishmania braziliensis | 99% | 100% |
A4HTM0 | Leishmania infantum | 47% | 100% |
A4HTM1 | Leishmania infantum | 46% | 92% |
A4IA57 | Leishmania infantum | 69% | 100% |
C6K3V8 | Leptomonas seymouri | 47% | 96% |
C6K3V9 | Leptomonas seymouri | 44% | 89% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 87% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 93% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 96% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 92% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q1U8 | Leishmania major | 42% | 100% |
Q4Q2R4 | Leishmania major | 70% | 100% |
Q4Q310 | Leishmania major | 43% | 100% |
Q4Q312 | Leishmania major | 42% | 100% |
Q4Q340 | Leishmania major | 43% | 100% |
Q4Q342 | Leishmania major | 43% | 100% |
Q4QI90 | Leishmania major | 43% | 100% |
Q4QI91 | Leishmania major | 46% | 99% |