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: A0A3Q8IMW3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.478 |
CLV_PCSK_FUR_1 | 508 | 512 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.482 |
CLV_PCSK_PC7_1 | 277 | 283 | PF00082 | 0.446 |
CLV_PCSK_PC7_1 | 506 | 512 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.557 |
CLV_Separin_Metazoa | 472 | 476 | PF03568 | 0.439 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.649 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.547 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.639 |
DOC_CYCLIN_yCln2_LP_2 | 193 | 199 | PF00134 | 0.430 |
DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 334 | 341 | PF00069 | 0.413 |
DOC_MAPK_NFAT4_5 | 334 | 342 | PF00069 | 0.438 |
DOC_PP1_RVXF_1 | 441 | 447 | PF00149 | 0.452 |
DOC_PP4_FxxP_1 | 342 | 345 | PF00568 | 0.472 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 162 | 166 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 13 | 17 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 508 | 516 | PF00244 | 0.555 |
LIG_Actin_WH2_2 | 134 | 151 | PF00022 | 0.611 |
LIG_Actin_WH2_2 | 203 | 219 | PF00022 | 0.399 |
LIG_APCC_ABBA_1 | 339 | 344 | PF00400 | 0.475 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.501 |
LIG_Clathr_ClatBox_1 | 347 | 351 | PF01394 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 340 | 350 | PF00928 | 0.403 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.593 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.544 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.309 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.750 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.542 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.307 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.636 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.545 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.586 |
LIG_GBD_Chelix_1 | 237 | 245 | PF00786 | 0.348 |
LIG_LIR_Apic_2 | 340 | 345 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.462 |
LIG_PCNA_yPIPBox_3 | 328 | 342 | PF02747 | 0.483 |
LIG_SH2_SRC | 470 | 473 | PF00017 | 0.519 |
LIG_SH2_SRC | 496 | 499 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 470 | 474 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.523 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.633 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.712 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.608 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.650 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.795 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 269 | 274 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 35 | 42 | PF11976 | 0.625 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.642 |
LIG_TRAF2_1 | 34 | 37 | PF00917 | 0.718 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.748 |
LIG_UBA3_1 | 480 | 485 | PF00899 | 0.514 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.713 |
MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.644 |
MOD_CDK_SPxxK_3 | 318 | 325 | PF00069 | 0.410 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.499 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.621 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.671 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.580 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.668 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.731 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.658 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.618 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.657 |
MOD_GlcNHglycan | 20 | 24 | PF01048 | 0.554 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.726 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.514 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.486 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.725 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.727 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.666 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.484 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.568 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.539 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.483 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.378 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.725 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.600 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.570 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.678 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.754 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.729 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.514 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.642 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.480 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.543 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.509 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.580 |
MOD_PIKK_1 | 418 | 424 | PF00454 | 0.426 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.555 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.608 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.678 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.560 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.385 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.515 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.700 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.718 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.557 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.560 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.540 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.740 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.723 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.558 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.704 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.671 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.721 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.729 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.494 |
MOD_SUMO_for_1 | 484 | 487 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_2 | 441 | 447 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_4 | 243 | 249 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 470 | 473 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3P7 | Leptomonas seymouri | 58% | 95% |
A0A0S4J1F8 | Bodo saltans | 26% | 95% |
A0A1X0NW49 | Trypanosomatidae | 33% | 100% |
A0A422NWS4 | Trypanosoma rangeli | 34% | 100% |
A4HDQ4 | Leishmania braziliensis | 87% | 100% |
A4I100 | Leishmania infantum | 100% | 100% |
C9ZWA9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AX38 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QAD8 | Leishmania major | 96% | 100% |