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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q918
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.368 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.615 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.565 |
CLV_PCSK_PC7_1 | 252 | 258 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.417 |
DEG_APCC_DBOX_1 | 35 | 43 | PF00400 | 0.545 |
DEG_APCC_DBOX_1 | 428 | 436 | PF00400 | 0.384 |
DEG_APCC_DBOX_1 | 514 | 522 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 344 | 348 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.607 |
DOC_ANK_TNKS_1 | 401 | 408 | PF00023 | 0.469 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.450 |
DOC_MAPK_DCC_7 | 136 | 145 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 136 | 145 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 260 | 270 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 136 | 145 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 263 | 272 | PF00069 | 0.484 |
DOC_MAPK_RevD_3 | 141 | 155 | PF00069 | 0.487 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.455 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.496 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.405 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 128 | 135 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 489 | 494 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 515 | 519 | PF00244 | 0.503 |
LIG_APCC_ABBA_1 | 384 | 389 | PF00400 | 0.419 |
LIG_BIR_III_2 | 452 | 456 | PF00653 | 0.443 |
LIG_BIR_III_4 | 164 | 168 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.377 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.469 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.494 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.480 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.603 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.443 |
LIG_LIR_Apic_2 | 172 | 177 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 370 | 380 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 181 | 186 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.387 |
LIG_MYND_3 | 518 | 522 | PF01753 | 0.524 |
LIG_NRBOX | 208 | 214 | PF00104 | 0.358 |
LIG_NRBOX | 503 | 509 | PF00104 | 0.432 |
LIG_PCNA_yPIPBox_3 | 206 | 218 | PF02747 | 0.406 |
LIG_Pex14_2 | 372 | 376 | PF04695 | 0.477 |
LIG_RPA_C_Fungi | 150 | 162 | PF08784 | 0.462 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.595 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 83 | 87 | PF00017 | 0.595 |
LIG_SH2_PTP2 | 142 | 145 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.385 |
LIG_SH3_1 | 98 | 104 | PF00018 | 0.629 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.508 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.700 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.708 |
LIG_SUMO_SIM_par_1 | 363 | 368 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 59 | 66 | PF11976 | 0.442 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.701 |
LIG_TYR_ITIM | 140 | 145 | PF00017 | 0.369 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.648 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.723 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.386 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.394 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.404 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.552 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.512 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.694 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.684 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.480 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.462 |
MOD_GlcNHglycan | 242 | 246 | PF01048 | 0.580 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.474 |
MOD_GlcNHglycan | 406 | 410 | PF01048 | 0.687 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.417 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.563 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.817 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.514 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.436 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.599 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.569 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.612 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.771 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.412 |
MOD_N-GLC_2 | 360 | 362 | PF02516 | 0.405 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.503 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.441 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.449 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.384 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.502 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.612 |
MOD_OFUCOSY | 362 | 369 | PF10250 | 0.398 |
MOD_PK_1 | 82 | 88 | PF00069 | 0.505 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.594 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.498 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.584 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.471 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.639 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.476 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.480 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.631 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.669 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.762 |
MOD_SUMO_for_1 | 470 | 473 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 392 | 400 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 494 | 499 | PF00179 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.583 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 77 | 79 | PF00400 | 0.409 |
TRG_NES_CRM1_1 | 301 | 314 | PF08389 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.464 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU4 | Leptomonas seymouri | 55% | 100% |
A0A1X0P8W2 | Trypanosomatidae | 34% | 100% |
A0A3S7X019 | Leishmania donovani | 94% | 100% |
A0A422N4R1 | Trypanosoma rangeli | 30% | 100% |
A4HD54 | Leishmania braziliensis | 80% | 100% |
A4I2A7 | Leishmania infantum | 94% | 100% |
C9ZXD5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AYF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BF90 | Trypanosoma cruzi | 34% | 100% |