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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9B4U4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 518 | 522 | PF00656 | 0.621 |
CLV_C14_Caspase3-7 | 524 | 528 | PF00656 | 0.601 |
CLV_MEL_PAP_1 | 153 | 159 | PF00089 | 0.551 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 552 | 554 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 71 | 73 | PF00082 | 0.540 |
CLV_PCSK_PC7_1 | 475 | 481 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.623 |
DEG_APCC_DBOX_1 | 48 | 56 | PF00400 | 0.494 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.581 |
DEG_SPOP_SBC_1 | 340 | 344 | PF00917 | 0.545 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.611 |
DOC_CKS1_1 | 58 | 63 | PF01111 | 0.473 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 311 | 318 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 23 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 384 | 391 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 88 | 98 | PF00069 | 0.533 |
DOC_MAPK_HePTP_8 | 153 | 165 | PF00069 | 0.549 |
DOC_MAPK_HePTP_8 | 414 | 430 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 133 | 140 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 156 | 165 | PF00069 | 0.550 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.524 |
DOC_PP2B_LxvP_1 | 338 | 341 | PF13499 | 0.564 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.427 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.659 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 15 | 23 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 156 | 160 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 222 | 230 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 269 | 275 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.621 |
LIG_BRCT_BRCA1_1 | 254 | 258 | PF00533 | 0.453 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.390 |
LIG_eIF4E_1 | 494 | 500 | PF01652 | 0.568 |
LIG_EVH1_2 | 128 | 132 | PF00568 | 0.446 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.777 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.588 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.553 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.463 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.623 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.735 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.611 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.481 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.482 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.467 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.588 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.593 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.500 |
LIG_LIR_Nem_3 | 421 | 426 | PF02991 | 0.559 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 231 | 235 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.473 |
LIG_SH3_2 | 121 | 126 | PF14604 | 0.617 |
LIG_SH3_2 | 67 | 72 | PF14604 | 0.492 |
LIG_SH3_3 | 118 | 124 | PF00018 | 0.667 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.653 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.644 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.639 |
LIG_SUMO_SIM_anti_2 | 425 | 430 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 109 | 114 | PF11976 | 0.666 |
LIG_SUMO_SIM_par_1 | 369 | 375 | PF11976 | 0.550 |
LIG_SxIP_EBH_1 | 115 | 125 | PF03271 | 0.541 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.616 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.506 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.656 |
LIG_TRFH_1 | 132 | 136 | PF08558 | 0.425 |
LIG_WW_3 | 119 | 123 | PF00397 | 0.581 |
LIG_WW_3 | 21 | 25 | PF00397 | 0.450 |
MOD_CDK_SPK_2 | 534 | 539 | PF00069 | 0.626 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.772 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.597 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.652 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.625 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.583 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.665 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.453 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.471 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.624 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.420 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.488 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.485 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.762 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.454 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.489 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.506 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.637 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.688 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.496 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.687 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.621 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.519 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.568 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.564 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.615 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.761 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.608 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.641 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.666 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.624 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.452 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.404 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.676 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.761 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.805 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.756 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.656 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.528 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.716 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.579 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.581 |
MOD_NEK2_2 | 155 | 160 | PF00069 | 0.541 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.525 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.478 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.710 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.583 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.541 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.486 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.637 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.578 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.597 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.714 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.490 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.346 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.565 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.502 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.646 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.622 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.574 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.642 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 297 | 307 | PF00179 | 0.539 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 551 | 553 | PF00400 | 0.530 |
TRG_NLS_Bipartite_1 | 417 | 438 | PF00514 | 0.375 |
TRG_NLS_MonoExtC_3 | 433 | 438 | PF00514 | 0.420 |
TRG_NLS_MonoExtN_4 | 431 | 438 | PF00514 | 0.412 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY58 | Leptomonas seymouri | 43% | 100% |
A0A3Q8II15 | Leishmania donovani | 86% | 100% |
A0A422MPI6 | Trypanosoma rangeli | 24% | 100% |
A4HBJ3 | Leishmania braziliensis | 63% | 99% |
A4I9T3 | Leishmania infantum | 87% | 100% |
C9ZMU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
Q4Q382 | Leishmania major | 86% | 100% |
V5BIT8 | Trypanosoma cruzi | 22% | 100% |