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: E9AQM6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 610 | 614 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.513 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 658 | 660 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 536 | 538 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 658 | 660 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.746 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.561 |
CLV_Separin_Metazoa | 303 | 307 | PF03568 | 0.222 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.740 |
DEG_SCF_FBW7_1 | 556 | 563 | PF00400 | 0.714 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.436 |
DEG_SPOP_SBC_1 | 560 | 564 | PF00917 | 0.776 |
DOC_MAPK_gen_1 | 574 | 583 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 515 | 522 | PF00069 | 0.386 |
DOC_MAPK_NFAT4_5 | 515 | 523 | PF00069 | 0.294 |
DOC_PP1_RVXF_1 | 513 | 520 | PF00149 | 0.403 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.819 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.611 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 125 | 131 | PF00244 | 0.811 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 411 | 416 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 491 | 500 | PF00244 | 0.352 |
LIG_Actin_WH2_2 | 637 | 654 | PF00022 | 0.437 |
LIG_BIR_III_4 | 162 | 166 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.611 |
LIG_Clathr_ClatBox_1 | 307 | 311 | PF01394 | 0.513 |
LIG_deltaCOP1_diTrp_1 | 656 | 660 | PF00928 | 0.460 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.547 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.603 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.387 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.285 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.448 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.620 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.501 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.744 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.700 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.350 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.622 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.693 |
LIG_Integrin_RGD_1 | 547 | 549 | PF01839 | 0.709 |
LIG_LIR_Apic_2 | 505 | 510 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 402 | 409 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 469 | 477 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 569 | 576 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 469 | 474 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 569 | 573 | PF02991 | 0.569 |
LIG_LRP6_Inhibitor_1 | 472 | 478 | PF00058 | 0.373 |
LIG_MAD2 | 392 | 400 | PF02301 | 0.325 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.762 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.411 |
LIG_Pex14_2 | 343 | 347 | PF04695 | 0.582 |
LIG_Rb_LxCxE_1 | 181 | 201 | PF01857 | 0.698 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.391 |
LIG_SH2_CRK | 507 | 511 | PF00017 | 0.502 |
LIG_SH2_GRB2like | 459 | 462 | PF00017 | 0.555 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 460 | 464 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.684 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.569 |
LIG_SH3_2 | 29 | 34 | PF14604 | 0.581 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.566 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.736 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.347 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.439 |
LIG_SUMO_SIM_anti_2 | 580 | 585 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 285 | 293 | PF11976 | 0.513 |
LIG_TYR_ITIM | 403 | 408 | PF00017 | 0.333 |
LIG_UBA3_1 | 517 | 524 | PF00899 | 0.339 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.436 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.600 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.600 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.726 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.336 |
MOD_CK1_1 | 555 | 561 | PF00069 | 0.713 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.677 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.604 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.652 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.478 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.332 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.250 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.566 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.500 |
MOD_CMANNOS | 498 | 501 | PF00535 | 0.448 |
MOD_CMANNOS | 657 | 660 | PF00535 | 0.590 |
MOD_DYRK1A_RPxSP_1 | 379 | 383 | PF00069 | 0.453 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.796 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.545 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.708 |
MOD_GlcNHglycan | 223 | 227 | PF01048 | 0.765 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.300 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.373 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.458 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.638 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.709 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.691 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.476 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.333 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.617 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.576 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.705 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.793 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.695 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.784 |
MOD_LATS_1 | 123 | 129 | PF00433 | 0.800 |
MOD_N-GLC_2 | 493 | 495 | PF02516 | 0.284 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.730 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.705 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.720 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.513 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.329 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.309 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.514 |
MOD_NEK2_2 | 234 | 239 | PF00069 | 0.488 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.598 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.719 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.574 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.503 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.520 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.375 |
MOD_Plk_1 | 428 | 434 | PF00069 | 0.712 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.486 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.448 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.674 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.636 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.411 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.503 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.397 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.729 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.754 |
MOD_SUMO_rev_2 | 342 | 351 | PF00179 | 0.440 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_2 | 264 | 270 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.458 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUK6 | Leptomonas seymouri | 33% | 100% |
A0A3S7WTX7 | Leishmania donovani | 78% | 98% |
A4H8I9 | Leishmania braziliensis | 57% | 100% |
E9AGN3 | Leishmania infantum | 78% | 98% |
Q4QEV2 | Leishmania major | 77% | 100% |