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: Q4Q437
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 422 | 426 | PF00656 | 0.585 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.537 |
CLV_PCSK_FUR_1 | 391 | 395 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.522 |
CLV_Separin_Metazoa | 211 | 215 | PF03568 | 0.647 |
CLV_Separin_Metazoa | 437 | 441 | PF03568 | 0.579 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.537 |
DEG_SPOP_SBC_1 | 187 | 191 | PF00917 | 0.698 |
DEG_SPOP_SBC_1 | 482 | 486 | PF00917 | 0.756 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.676 |
DOC_CYCLIN_RxL_1 | 340 | 351 | PF00134 | 0.568 |
DOC_MAPK_MEF2A_6 | 2 | 9 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.481 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.599 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.647 |
DOC_USP7_MATH_2 | 313 | 319 | PF00917 | 0.550 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 126 | 134 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 214 | 221 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 243 | 251 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 369 | 375 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 492 | 499 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.527 |
LIG_Actin_WH2_2 | 227 | 245 | PF00022 | 0.542 |
LIG_Actin_WH2_2 | 377 | 395 | PF00022 | 0.541 |
LIG_Actin_WH2_2 | 453 | 468 | PF00022 | 0.475 |
LIG_Actin_WH2_2 | 518 | 534 | PF00022 | 0.496 |
LIG_APCC_ABBA_1 | 5 | 10 | PF00400 | 0.548 |
LIG_APCC_ABBA_1 | 507 | 512 | PF00400 | 0.480 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.614 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.630 |
LIG_deltaCOP1_diTrp_1 | 300 | 308 | PF00928 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 502 | 510 | PF00928 | 0.603 |
LIG_EVH1_1 | 179 | 183 | PF00568 | 0.590 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.577 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.617 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.495 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.620 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.495 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.527 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.773 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.556 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.697 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.581 |
LIG_FHA_2 | 579 | 585 | PF00498 | 0.829 |
LIG_LIR_Apic_2 | 584 | 590 | PF02991 | 0.702 |
LIG_LIR_Gen_1 | 152 | 161 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 271 | 281 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.608 |
LIG_LYPXL_yS_3 | 448 | 451 | PF13949 | 0.493 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.577 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.531 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.668 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.606 |
LIG_SH2_CRK | 429 | 433 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 274 | 278 | PF00017 | 0.688 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.520 |
LIG_SH2_SRC | 102 | 105 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.688 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.506 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.672 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.650 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.613 |
LIG_Sin3_3 | 71 | 78 | PF02671 | 0.628 |
LIG_SUMO_SIM_anti_2 | 344 | 349 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 182 | 191 | PF11976 | 0.593 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.787 |
LIG_TYR_ITIM | 446 | 451 | PF00017 | 0.508 |
MOD_CDK_SPxxK_3 | 362 | 369 | PF00069 | 0.722 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.685 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.704 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.655 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.767 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.363 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.613 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.754 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.573 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.534 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.777 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.798 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.562 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.657 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.604 |
MOD_CK2_1 | 578 | 584 | PF00069 | 0.810 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.583 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.548 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.691 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.579 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.565 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.620 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.749 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.440 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.489 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.667 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.547 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.434 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.664 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.583 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.519 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.567 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.741 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.680 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.691 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.735 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.752 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.403 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.565 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.538 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.563 |
MOD_LATS_1 | 453 | 459 | PF00433 | 0.470 |
MOD_N-GLC_1 | 261 | 266 | PF02516 | 0.840 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.566 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.594 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.507 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.526 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.502 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.614 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.685 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.632 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.735 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.597 |
MOD_PIKK_1 | 603 | 609 | PF00454 | 0.593 |
MOD_PK_1 | 376 | 382 | PF00069 | 0.596 |
MOD_PKA_1 | 214 | 220 | PF00069 | 0.704 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.808 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.704 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.676 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.548 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.537 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.541 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.614 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.620 |
MOD_PKB_1 | 214 | 222 | PF00069 | 0.705 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.595 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.711 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.406 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.541 |
MOD_Plk_2-3 | 139 | 145 | PF00069 | 0.662 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.556 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.521 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.537 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.472 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.385 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.682 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.772 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.493 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.721 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.566 |
MOD_SUMO_for_1 | 14 | 17 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 257 | 265 | PF00179 | 0.704 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 446 | 451 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 526 | 531 | PF01217 | 0.469 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.265 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 391 | 394 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 491 | 494 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 235 | 239 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 310 | 315 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 529 | 533 | PF00026 | 0.487 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P490 | Leptomonas seymouri | 37% | 100% |
A0A3Q8IGM0 | Leishmania donovani | 88% | 100% |
A4HLL1 | Leishmania braziliensis | 71% | 100% |
A4I923 | Leishmania infantum | 87% | 100% |
E9B3Y7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |