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: 36 |
NetGPI | no | yes: 0, no: 36 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 17 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
Related structures:
AlphaFold database: A4H5D0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.381 |
CLV_C14_Caspase3-7 | 556 | 560 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.616 |
CLV_PCSK_FUR_1 | 239 | 243 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.598 |
DEG_APCC_DBOX_1 | 495 | 503 | PF00400 | 0.245 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.573 |
DOC_ANK_TNKS_1 | 547 | 554 | PF00023 | 0.297 |
DOC_MAPK_DCC_7 | 52 | 62 | PF00069 | 0.477 |
DOC_MAPK_DCC_7 | 67 | 77 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 150 | 160 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 185 | 194 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 435 | 442 | PF00069 | 0.283 |
DOC_MAPK_gen_1 | 44 | 50 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 353 | 361 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 407 | 415 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 435 | 444 | PF00069 | 0.292 |
DOC_PP1_RVXF_1 | 456 | 462 | PF00149 | 0.336 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 378 | 381 | PF13499 | 0.369 |
DOC_PP2B_PxIxI_1 | 330 | 336 | PF00149 | 0.305 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.648 |
DOC_SPAK_OSR1_1 | 282 | 286 | PF12202 | 0.382 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.229 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.679 |
DOC_USP7_MATH_2 | 513 | 519 | PF00917 | 0.268 |
DOC_USP7_UBL2_3 | 539 | 543 | PF12436 | 0.382 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.293 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 141 | 151 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 270 | 279 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 399 | 404 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 423 | 431 | PF00244 | 0.220 |
LIG_14-3-3_CanoR_1 | 586 | 596 | PF00244 | 0.363 |
LIG_Actin_WH2_2 | 357 | 374 | PF00022 | 0.355 |
LIG_BIR_III_4 | 103 | 107 | PF00653 | 0.559 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.274 |
LIG_deltaCOP1_diTrp_1 | 316 | 323 | PF00928 | 0.372 |
LIG_deltaCOP1_diTrp_1 | 579 | 583 | PF00928 | 0.333 |
LIG_eIF4E_1 | 516 | 522 | PF01652 | 0.320 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.562 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.573 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.466 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.287 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.425 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.543 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.372 |
LIG_LIR_Apic_2 | 17 | 22 | PF02991 | 0.654 |
LIG_LIR_Apic_2 | 316 | 321 | PF02991 | 0.252 |
LIG_LIR_Apic_2 | 460 | 465 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 156 | 164 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 123 | 127 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 156 | 160 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.555 |
LIG_NRBOX | 498 | 504 | PF00104 | 0.334 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.312 |
LIG_Pex14_2 | 62 | 66 | PF04695 | 0.610 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.451 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.371 |
LIG_SH2_CRK | 574 | 578 | PF00017 | 0.370 |
LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 462 | 466 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 574 | 578 | PF00017 | 0.365 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.534 |
LIG_SH3_1 | 67 | 73 | PF00018 | 0.533 |
LIG_SH3_2 | 40 | 45 | PF14604 | 0.546 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.645 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.669 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.312 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.540 |
LIG_SUMO_SIM_anti_2 | 408 | 414 | PF11976 | 0.287 |
LIG_SUMO_SIM_par_1 | 332 | 337 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 358 | 363 | PF11976 | 0.230 |
LIG_TYR_ITIM | 572 | 577 | PF00017 | 0.410 |
MOD_CDC14_SPxK_1 | 42 | 45 | PF00782 | 0.408 |
MOD_CDK_SPK_2 | 39 | 44 | PF00069 | 0.421 |
MOD_CDK_SPxK_1 | 39 | 45 | PF00069 | 0.413 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.304 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.331 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.549 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.475 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.575 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.420 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.375 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.478 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.569 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.435 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.431 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.283 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.354 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.523 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.339 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.267 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.439 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.424 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.569 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.340 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.443 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.425 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.396 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.406 |
MOD_NEK2_2 | 260 | 265 | PF00069 | 0.290 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.354 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.440 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.436 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.376 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.444 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.375 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.416 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.321 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.413 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.332 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.448 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.393 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.462 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.475 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.414 |
TRG_DiLeu_BaLyEn_6 | 517 | 522 | PF01217 | 0.294 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.524 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 43 | 45 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 509 | 511 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 583 | 586 | PF00400 | 0.257 |
TRG_NES_CRM1_1 | 355 | 369 | PF08389 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 229 | 234 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 286 | 291 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN2 | Leptomonas seymouri | 40% | 91% |
A0A0N1PB02 | Leptomonas seymouri | 49% | 91% |
A0A0S4J6C6 | Bodo saltans | 42% | 92% |
A0A1X0P9A6 | Trypanosomatidae | 44% | 87% |
A0A3Q8IHH1 | Leishmania donovani | 40% | 82% |
A0A3R7K2Y9 | Trypanosoma rangeli | 49% | 87% |
A0A3S5H668 | Leishmania donovani | 44% | 100% |
A0A3S5H669 | Leishmania donovani | 75% | 94% |
A0A3S7X835 | Leishmania donovani | 44% | 100% |
A4H5C9 | Leishmania braziliensis | 44% | 100% |
A4HAZ7 | Leishmania braziliensis | 45% | 100% |
A4HAZ9 | Leishmania braziliensis | 47% | 96% |
A4HB01 | Leishmania braziliensis | 47% | 100% |
A4HTM0 | Leishmania infantum | 46% | 100% |
A4HTM1 | Leishmania infantum | 75% | 94% |
A4IA57 | Leishmania infantum | 45% | 100% |
C6K3V8 | Leptomonas seymouri | 42% | 98% |
C6K3V9 | Leptomonas seymouri | 66% | 91% |
C9ZMY5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 88% |
E8NHE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 94% |
E8NHF6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 98% |
E8NHR9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AME6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AME7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 94% |
E9B571 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
Q4Q1U8 | Leishmania major | 40% | 100% |
Q4Q2R4 | Leishmania major | 46% | 100% |
Q4Q310 | Leishmania major | 40% | 100% |
Q4Q312 | Leishmania major | 40% | 100% |
Q4Q340 | Leishmania major | 40% | 100% |
Q4Q342 | Leishmania major | 40% | 100% |
Q4QI90 | Leishmania major | 73% | 100% |
Q4QI91 | Leishmania major | 44% | 97% |