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: E9AMY0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.528 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.666 |
CLV_C14_Caspase3-7 | 46 | 50 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.490 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.765 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.394 |
DEG_COP1_1 | 264 | 273 | PF00400 | 0.691 |
DEG_SCF_FBW7_1 | 468 | 475 | PF00400 | 0.512 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.516 |
DEG_SPOP_SBC_1 | 273 | 277 | PF00917 | 0.679 |
DOC_ANK_TNKS_1 | 186 | 193 | PF00023 | 0.405 |
DOC_CYCLIN_RxL_1 | 221 | 232 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 484 | 492 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 384 | 393 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 484 | 492 | PF00069 | 0.414 |
DOC_PP1_RVXF_1 | 222 | 229 | PF00149 | 0.458 |
DOC_PP1_RVXF_1 | 482 | 488 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 490 | 493 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 534 | 537 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.583 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.484 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.509 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 334 | 342 | PF00244 | 0.603 |
LIG_Actin_WH2_2 | 214 | 229 | PF00022 | 0.451 |
LIG_BIR_III_4 | 442 | 446 | PF00653 | 0.433 |
LIG_BIR_III_4 | 553 | 557 | PF00653 | 0.653 |
LIG_CSL_BTD_1 | 387 | 390 | PF09270 | 0.403 |
LIG_deltaCOP1_diTrp_1 | 145 | 156 | PF00928 | 0.496 |
LIG_EABR_CEP55_1 | 15 | 24 | PF12180 | 0.575 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.468 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.667 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.566 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.432 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.591 |
LIG_FHA_2 | 469 | 475 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 99 | 107 | PF02991 | 0.564 |
LIG_LIR_LC3C_4 | 434 | 438 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.521 |
LIG_MAD2 | 392 | 400 | PF02301 | 0.443 |
LIG_MYND_1 | 278 | 282 | PF01753 | 0.662 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.447 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.532 |
LIG_SH2_PTP2 | 302 | 305 | PF00017 | 0.335 |
LIG_SH2_SRC | 172 | 175 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.386 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.756 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.585 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.676 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.494 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.380 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 434 | 439 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 302 | 307 | PF11976 | 0.254 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.506 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.623 |
LIG_WRC_WIRS_1 | 107 | 112 | PF05994 | 0.447 |
LIG_WW_3 | 287 | 291 | PF00397 | 0.484 |
MOD_CDC14_SPxK_1 | 343 | 346 | PF00782 | 0.643 |
MOD_CDK_SPK_2 | 274 | 279 | PF00069 | 0.772 |
MOD_CDK_SPxK_1 | 340 | 346 | PF00069 | 0.636 |
MOD_CDK_SPxxK_3 | 340 | 347 | PF00069 | 0.639 |
MOD_CDK_SPxxK_3 | 415 | 422 | PF00069 | 0.471 |
MOD_CDK_SPxxK_3 | 79 | 86 | PF00069 | 0.424 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.664 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.538 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.396 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.577 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.509 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.561 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.621 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.500 |
MOD_CMANNOS | 156 | 159 | PF00535 | 0.459 |
MOD_Cter_Amidation | 344 | 347 | PF01082 | 0.714 |
MOD_DYRK1A_RPxSP_1 | 340 | 344 | PF00069 | 0.629 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.621 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.604 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.720 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.699 |
MOD_GlcNHglycan | 25 | 30 | PF01048 | 0.493 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.439 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.632 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.731 |
MOD_GlcNHglycan | 363 | 367 | PF01048 | 0.634 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.509 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.446 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.453 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.591 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.511 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.575 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.623 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.505 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.426 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.638 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.584 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.597 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.430 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.647 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.381 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.643 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.641 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.475 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.440 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.415 |
MOD_PKA_1 | 334 | 340 | PF00069 | 0.622 |
MOD_PKA_1 | 560 | 566 | PF00069 | 0.755 |
MOD_PKA_2 | 560 | 566 | PF00069 | 0.755 |
MOD_PKB_1 | 332 | 340 | PF00069 | 0.475 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.464 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.556 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.403 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.507 |
MOD_Plk_4 | 495 | 501 | PF00069 | 0.476 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.460 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.543 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.684 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.636 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.583 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.524 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.604 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.480 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.521 |
MOD_SUMO_rev_2 | 351 | 358 | PF00179 | 0.669 |
MOD_SUMO_rev_2 | 377 | 385 | PF00179 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 221 | 226 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2D8 | Leptomonas seymouri | 39% | 89% |
A0A1X0NIM5 | Trypanosomatidae | 27% | 94% |
A0A3Q8I7J7 | Leishmania donovani | 88% | 99% |
A4HU51 | Leishmania infantum | 88% | 99% |
Q4QHP6 | Leishmania major | 85% | 100% |