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: A4HDU6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.467 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.479 |
DEG_SCF_FBW7_1 | 434 | 439 | PF00400 | 0.563 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.560 |
DOC_CKS1_1 | 433 | 438 | PF01111 | 0.564 |
DOC_MAPK_gen_1 | 134 | 140 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 481 | 488 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 448 | 456 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 462 | 471 | PF00069 | 0.496 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.600 |
DOC_PP4_FxxP_1 | 38 | 41 | PF00568 | 0.460 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.500 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.485 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 304 | 312 | PF00244 | 0.779 |
LIG_14-3-3_CanoR_1 | 385 | 394 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.635 |
LIG_Actin_WH2_2 | 123 | 141 | PF00022 | 0.407 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.383 |
LIG_APCC_ABBA_1 | 166 | 171 | PF00400 | 0.416 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.549 |
LIG_CtBP_PxDLS_1 | 468 | 472 | PF00389 | 0.548 |
LIG_DLG_GKlike_1 | 448 | 456 | PF00625 | 0.602 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.336 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.469 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.391 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.402 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.472 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.514 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.537 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.529 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.462 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 187 | 192 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 272 | 278 | PF02991 | 0.643 |
LIG_LIR_Apic_2 | 92 | 97 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 107 | 117 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 11 | 22 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 30 | 41 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.563 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.326 |
LIG_Pex14_1 | 33 | 37 | PF04695 | 0.451 |
LIG_PTAP_UEV_1 | 356 | 361 | PF05743 | 0.508 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.638 |
LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.629 |
LIG_SH2_SRC | 190 | 193 | PF00017 | 0.416 |
LIG_SH2_STAT3 | 201 | 204 | PF00017 | 0.376 |
LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.465 |
LIG_SH3_1 | 462 | 468 | PF00018 | 0.517 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.416 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.489 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.754 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.704 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.517 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.472 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.614 |
LIG_SUMO_SIM_anti_2 | 125 | 132 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 125 | 132 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 467 | 473 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 484 | 489 | PF11976 | 0.521 |
LIG_SxIP_EBH_1 | 385 | 398 | PF03271 | 0.525 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.617 |
LIG_TRFH_1 | 37 | 41 | PF08558 | 0.459 |
LIG_TRFH_1 | 420 | 424 | PF08558 | 0.527 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.455 |
MOD_CDK_SPK_2 | 476 | 481 | PF00069 | 0.559 |
MOD_CDK_SPxxK_3 | 476 | 483 | PF00069 | 0.572 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.461 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.543 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.468 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.405 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.612 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.653 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.650 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.622 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.543 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.559 |
MOD_Cter_Amidation | 366 | 369 | PF01082 | 0.528 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.539 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.440 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.387 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.558 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.571 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.618 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.535 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.525 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.513 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.619 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.463 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.289 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.509 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.550 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.459 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.674 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.598 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.629 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.668 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.443 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.436 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.448 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.375 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.459 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.745 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.612 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.542 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.643 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.681 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.463 |
MOD_NEK2_2 | 18 | 23 | PF00069 | 0.457 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.455 |
MOD_PIKK_1 | 426 | 432 | PF00454 | 0.592 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.529 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.556 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.557 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.490 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.599 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.445 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.408 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.532 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.685 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.523 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.541 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.585 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.460 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.595 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.586 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.428 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.472 |
MOD_SUMO_rev_2 | 174 | 184 | PF00179 | 0.467 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEP2 | Leptomonas seymouri | 34% | 100% |
A0A3S7WY45 | Leishmania donovani | 61% | 100% |
A4I0N7 | Leishmania infantum | 61% | 100% |
E9AWN7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QAT4 | Leishmania major | 61% | 98% |