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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HEW3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.664 |
CLV_MEL_PAP_1 | 249 | 255 | PF00089 | 0.617 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.514 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.734 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.774 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.623 |
CLV_Separin_Metazoa | 120 | 124 | PF03568 | 0.475 |
DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.782 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.541 |
DOC_CDC14_PxL_1 | 84 | 92 | PF14671 | 0.529 |
DOC_MAPK_MEF2A_6 | 352 | 360 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 361 | 368 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 441 | 448 | PF00069 | 0.304 |
DOC_PP2B_LxvP_1 | 173 | 176 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 550 | 553 | PF13499 | 0.616 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 30 | 38 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 497 | 502 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 83 | 88 | PF00244 | 0.538 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.723 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.665 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.728 |
LIG_BRCT_BRCA1_1 | 310 | 314 | PF00533 | 0.423 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.541 |
LIG_deltaCOP1_diTrp_1 | 242 | 246 | PF00928 | 0.622 |
LIG_deltaCOP1_diTrp_1 | 279 | 288 | PF00928 | 0.586 |
LIG_EH_1 | 227 | 231 | PF12763 | 0.484 |
LIG_eIF4E_1 | 310 | 316 | PF01652 | 0.283 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.663 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.664 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.531 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.435 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.563 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.516 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.584 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.510 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.602 |
LIG_LIR_Gen_1 | 16 | 24 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 242 | 251 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.606 |
LIG_MYND_3 | 164 | 168 | PF01753 | 0.536 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.630 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.695 |
LIG_SH2_NCK_1 | 132 | 136 | PF00017 | 0.630 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.606 |
LIG_SH2_STAP1 | 233 | 237 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.284 |
LIG_SH2_STAT3 | 233 | 236 | PF00017 | 0.727 |
LIG_SH2_STAT3 | 346 | 349 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.547 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.579 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.570 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.533 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.535 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.791 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.802 |
LIG_SUMO_SIM_anti_2 | 421 | 427 | PF11976 | 0.491 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.738 |
LIG_TRAF2_1 | 287 | 290 | PF00917 | 0.492 |
LIG_TRFH_1 | 440 | 444 | PF08558 | 0.309 |
LIG_WRC_WIRS_1 | 498 | 503 | PF05994 | 0.504 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.739 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.723 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.647 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.665 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.390 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.732 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.507 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.703 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.662 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.640 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.656 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.710 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.580 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.558 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.568 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.719 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.662 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.787 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.734 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.619 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.671 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.585 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.813 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.642 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.691 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.745 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.652 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.691 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.481 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.463 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.578 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.461 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.425 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.600 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.633 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.541 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.677 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.665 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.681 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.706 |
MOD_LATS_1 | 35 | 41 | PF00433 | 0.586 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.464 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.734 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.722 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.323 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.685 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.564 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.438 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.552 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.438 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.679 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.682 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.470 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.433 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.729 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.538 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.727 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.717 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.717 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.576 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.542 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.623 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.581 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.729 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.684 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.495 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.627 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.652 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.537 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.774 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.714 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.650 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.690 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.577 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.639 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.586 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.755 |
TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.648 |
TRG_DiLeu_BaEn_2 | 442 | 448 | PF01217 | 0.551 |
TRG_DiLeu_BaLyEn_6 | 244 | 249 | PF01217 | 0.734 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.693 |
TRG_NLS_Bipartite_1 | 42 | 62 | PF00514 | 0.629 |
TRG_NLS_MonoExtN_4 | 56 | 62 | PF00514 | 0.800 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.730 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P648 | Leptomonas seymouri | 33% | 100% |
A0A3S7WZS1 | Leishmania donovani | 66% | 99% |
A4I236 | Leishmania infantum | 66% | 99% |
E9AY86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 99% |
Q4Q987 | Leishmania major | 67% | 100% |