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: 5 |
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: A0A3Q8IAX6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.628 |
CLV_PCSK_FUR_1 | 42 | 46 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.667 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.481 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.730 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.357 |
CLV_Separin_Metazoa | 258 | 262 | PF03568 | 0.685 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.746 |
DOC_CKS1_1 | 418 | 423 | PF01111 | 0.411 |
DOC_CYCLIN_RxL_1 | 222 | 230 | PF00134 | 0.695 |
DOC_CYCLIN_RxL_1 | 343 | 352 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 418 | 424 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 436 | 442 | PF00134 | 0.724 |
DOC_CYCLIN_yCln2_LP_2 | 72 | 78 | PF00134 | 0.781 |
DOC_MAPK_gen_1 | 357 | 363 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 87 | 95 | PF00069 | 0.710 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 30 | 37 | PF00069 | 0.638 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.643 |
DOC_PP2B_LxvP_1 | 510 | 513 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.810 |
DOC_PP2B_LxvP_1 | 93 | 96 | PF13499 | 0.745 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.786 |
LIG_14-3-3_CanoR_1 | 137 | 146 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 262 | 270 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 334 | 340 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 61 | 65 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.748 |
LIG_Actin_WH2_2 | 246 | 263 | PF00022 | 0.504 |
LIG_BIR_III_4 | 190 | 194 | PF00653 | 0.848 |
LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.685 |
LIG_FAT_LD_1 | 555 | 563 | PF03623 | 0.518 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.705 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.706 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.570 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.367 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.508 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.711 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.711 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.794 |
LIG_LIR_Gen_1 | 204 | 213 | PF02991 | 0.706 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.722 |
LIG_LIR_Gen_1 | 296 | 306 | PF02991 | 0.728 |
LIG_LIR_Gen_1 | 564 | 573 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 564 | 569 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 574 | 579 | PF02991 | 0.502 |
LIG_MAD2 | 137 | 145 | PF02301 | 0.632 |
LIG_MLH1_MIPbox_1 | 295 | 299 | PF16413 | 0.685 |
LIG_Pex14_1 | 295 | 299 | PF04695 | 0.657 |
LIG_Pex14_1 | 426 | 430 | PF04695 | 0.411 |
LIG_Pex14_2 | 208 | 212 | PF04695 | 0.706 |
LIG_Pex14_2 | 299 | 303 | PF04695 | 0.647 |
LIG_Pex14_2 | 485 | 489 | PF04695 | 0.653 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.512 |
LIG_SH2_CRK | 566 | 570 | PF00017 | 0.536 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.790 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.790 |
LIG_SH2_PTP2 | 196 | 199 | PF00017 | 0.761 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.761 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.789 |
LIG_SH3_1 | 196 | 202 | PF00018 | 0.753 |
LIG_SH3_1 | 237 | 243 | PF00018 | 0.706 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.762 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.706 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.533 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.756 |
LIG_SH3_CIN85_PxpxPR_1 | 439 | 444 | PF14604 | 0.678 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.683 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.757 |
LIG_TRAF2_1 | 16 | 19 | PF00917 | 0.789 |
LIG_TRFH_1 | 196 | 200 | PF08558 | 0.808 |
MOD_CDC14_SPxK_1 | 222 | 225 | PF00782 | 0.572 |
MOD_CDK_SPxK_1 | 219 | 225 | PF00069 | 0.574 |
MOD_CDK_SPxK_1 | 548 | 554 | PF00069 | 0.577 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.694 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.709 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.732 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.719 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.698 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.727 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.403 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.754 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.648 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.579 |
MOD_Cter_Amidation | 355 | 358 | PF01082 | 0.631 |
MOD_Cter_Amidation | 399 | 402 | PF01082 | 0.637 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.783 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.697 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.707 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.650 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.676 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.629 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.662 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.676 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.685 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.615 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.636 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.661 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.635 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.678 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.624 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.571 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.660 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.642 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.733 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.641 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.761 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.740 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.624 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.635 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.614 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.642 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.556 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.687 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.784 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.592 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.687 |
MOD_OFUCOSY | 509 | 516 | PF10250 | 0.471 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.755 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.467 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.660 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.580 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.650 |
MOD_PKA_1 | 401 | 407 | PF00069 | 0.622 |
MOD_PKA_1 | 44 | 50 | PF00069 | 0.687 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.597 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.480 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.620 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.811 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.655 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.706 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.597 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.639 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.552 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.796 |
MOD_PKB_1 | 42 | 50 | PF00069 | 0.683 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.775 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.692 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.733 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.585 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.688 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.689 |
MOD_Plk_4 | 571 | 577 | PF00069 | 0.606 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.770 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.411 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.577 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.748 |
MOD_SUMO_for_1 | 464 | 467 | PF00179 | 0.574 |
TRG_DiLeu_BaEn_3 | 342 | 348 | PF01217 | 0.601 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.598 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.753 |
TRG_Pf-PMV_PEXEL_1 | 107 | 112 | PF00026 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ42 | Leptomonas seymouri | 50% | 100% |
A4HYZ0 | Leishmania infantum | 97% | 100% |
E9AIK4 | Leishmania braziliensis | 75% | 98% |
E9AUT6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QCP7 | Leishmania major | 89% | 99% |