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: A0A3Q8IGM0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 423 | 427 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 506 | 510 | PF00656 | 0.347 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.508 |
CLV_PCSK_FUR_1 | 392 | 396 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.482 |
CLV_Separin_Metazoa | 212 | 216 | PF03568 | 0.657 |
CLV_Separin_Metazoa | 438 | 442 | PF03568 | 0.531 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.531 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.706 |
DOC_CDC14_PxL_1 | 158 | 166 | PF14671 | 0.645 |
DOC_CYCLIN_RxL_1 | 341 | 352 | PF00134 | 0.520 |
DOC_CYCLIN_RxL_1 | 370 | 380 | PF00134 | 0.436 |
DOC_CYCLIN_yCln2_LP_2 | 180 | 186 | PF00134 | 0.631 |
DOC_MAPK_gen_1 | 374 | 383 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 377 | 385 | PF00069 | 0.469 |
DOC_PP2B_LxvP_1 | 184 | 187 | PF13499 | 0.586 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.661 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 598 | 602 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.512 |
DOC_USP7_MATH_2 | 314 | 320 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.552 |
LIG_14-3-3_CanoR_1 | 215 | 222 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 244 | 252 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 370 | 378 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 392 | 402 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 493 | 500 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 579 | 587 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 88 | 96 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 228 | 246 | PF00022 | 0.521 |
LIG_Actin_WH2_2 | 378 | 396 | PF00022 | 0.495 |
LIG_Actin_WH2_2 | 454 | 469 | PF00022 | 0.402 |
LIG_Actin_WH2_2 | 519 | 535 | PF00022 | 0.429 |
LIG_APCC_ABBA_1 | 5 | 10 | PF00400 | 0.482 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 53 | 57 | PF00533 | 0.574 |
LIG_deltaCOP1_diTrp_1 | 301 | 309 | PF00928 | 0.494 |
LIG_deltaCOP1_diTrp_1 | 503 | 511 | PF00928 | 0.551 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.581 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.576 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.647 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.425 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.612 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.482 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.495 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.612 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.662 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.572 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.553 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.799 |
LIG_LIR_Gen_1 | 152 | 162 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 152 | 158 | PF02991 | 0.574 |
LIG_LYPXL_yS_3 | 449 | 452 | PF13949 | 0.441 |
LIG_NRBOX | 288 | 294 | PF00104 | 0.498 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.556 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.626 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 275 | 279 | PF00017 | 0.636 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.482 |
LIG_SH2_SRC | 103 | 106 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.636 |
LIG_SH2_STAP1 | 430 | 434 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.477 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.613 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.699 |
LIG_Sin3_3 | 72 | 79 | PF02671 | 0.601 |
LIG_SUMO_SIM_anti_2 | 345 | 350 | PF11976 | 0.508 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.735 |
LIG_TYR_ITIM | 447 | 452 | PF00017 | 0.563 |
MOD_CDK_SPxxK_3 | 363 | 370 | PF00069 | 0.656 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.615 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.625 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.632 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.717 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.439 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.619 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.700 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.531 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.723 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.738 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.609 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.481 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.788 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.453 |
MOD_Cter_Amidation | 571 | 574 | PF01082 | 0.593 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.516 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.374 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.775 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.650 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.507 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.499 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.697 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.551 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.422 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.422 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.404 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.609 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.495 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.380 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.620 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.321 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.545 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.503 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.581 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.741 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.653 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.661 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.609 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.643 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.701 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.684 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.397 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.518 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.468 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.496 |
MOD_LATS_1 | 454 | 460 | PF00433 | 0.397 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.784 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.527 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.448 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.425 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.517 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.427 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.571 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.635 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.581 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.726 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.557 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.562 |
MOD_PK_1 | 377 | 383 | PF00069 | 0.542 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.697 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.767 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.697 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.593 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.667 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.625 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.503 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.464 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.567 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.558 |
MOD_PKB_1 | 215 | 223 | PF00069 | 0.697 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.682 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.621 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.529 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.479 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.668 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.565 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.490 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.483 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.516 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.394 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.388 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.602 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.715 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.426 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.690 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.545 |
MOD_SUMO_for_1 | 14 | 17 | PF00179 | 0.504 |
TRG_DiLeu_BaEn_1 | 338 | 343 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 527 | 532 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.441 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 440 | 442 | PF00400 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 311 | 316 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 374 | 379 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 530 | 534 | PF00026 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P490 | Leptomonas seymouri | 36% | 100% |
A4HLL1 | Leishmania braziliensis | 71% | 98% |
A4I923 | Leishmania infantum | 100% | 100% |
E9B3Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q437 | Leishmania major | 88% | 100% |