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: A4H6G2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 68 | 74 | PF00089 | 0.633 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.548 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 609 | 611 | PF00082 | 0.610 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 590 | 592 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 609 | 611 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.587 |
DEG_APCC_DBOX_1 | 590 | 598 | PF00400 | 0.428 |
DEG_COP1_1 | 133 | 143 | PF00400 | 0.515 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.627 |
DEG_SPOP_SBC_1 | 19 | 23 | PF00917 | 0.609 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.527 |
DEG_SPOP_SBC_1 | 536 | 540 | PF00917 | 0.494 |
DOC_CKS1_1 | 186 | 191 | PF01111 | 0.521 |
DOC_CKS1_1 | 83 | 88 | PF01111 | 0.520 |
DOC_CYCLIN_RxL_1 | 588 | 595 | PF00134 | 0.583 |
DOC_MAPK_gen_1 | 225 | 234 | PF00069 | 0.608 |
DOC_MAPK_gen_1 | 293 | 303 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 296 | 305 | PF00069 | 0.521 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.665 |
DOC_PP2B_LxvP_1 | 555 | 558 | PF13499 | 0.521 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.488 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 228 | 234 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 433 | 441 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 591 | 597 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 610 | 618 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.567 |
LIG_Actin_WH2_2 | 264 | 282 | PF00022 | 0.593 |
LIG_BRCT_BRCA1_1 | 630 | 634 | PF00533 | 0.586 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.564 |
LIG_CaM_IQ_9 | 298 | 313 | PF13499 | 0.567 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.529 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.681 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.434 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.637 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.515 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.422 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.670 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.646 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.567 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.694 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.519 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.645 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.699 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.600 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.620 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.655 |
LIG_IRF3_LxIS_1 | 297 | 304 | PF10401 | 0.557 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 255 | 263 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 463 | 472 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 463 | 467 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 631 | 637 | PF02991 | 0.592 |
LIG_NRBOX | 551 | 557 | PF00104 | 0.444 |
LIG_PCNA_PIPBox_1 | 272 | 281 | PF02747 | 0.595 |
LIG_Pex14_1 | 151 | 155 | PF04695 | 0.457 |
LIG_Pex14_1 | 216 | 220 | PF04695 | 0.530 |
LIG_RPA_C_Fungi | 428 | 440 | PF08784 | 0.492 |
LIG_SH2_GRB2like | 548 | 551 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 637 | 641 | PF00017 | 0.621 |
LIG_SH2_STAT3 | 548 | 551 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.622 |
LIG_SH3_2 | 61 | 66 | PF14604 | 0.576 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.547 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.582 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.590 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.595 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.556 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.513 |
LIG_SH3_5 | 252 | 256 | PF00018 | 0.565 |
LIG_SUMO_SIM_anti_2 | 264 | 270 | PF11976 | 0.426 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.553 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.711 |
LIG_TRAF2_1 | 500 | 503 | PF00917 | 0.482 |
LIG_TRAF2_1 | 568 | 571 | PF00917 | 0.495 |
LIG_TYR_ITIM | 254 | 259 | PF00017 | 0.484 |
LIG_UBA3_1 | 585 | 590 | PF00899 | 0.433 |
LIG_WRC_WIRS_1 | 461 | 466 | PF05994 | 0.579 |
LIG_WW_3 | 293 | 297 | PF00397 | 0.604 |
MOD_CDK_SPK_2 | 614 | 619 | PF00069 | 0.484 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.525 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.692 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.553 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.607 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.562 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.541 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.627 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.686 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.536 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.615 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.557 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.537 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.668 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.573 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.493 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.469 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.699 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.586 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.661 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.738 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.658 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.579 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.758 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.770 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.615 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.566 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.451 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.574 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.548 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.639 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.709 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.549 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.596 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.602 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.459 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.676 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.602 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.703 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.539 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.437 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.481 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.680 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.602 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.542 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.709 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.707 |
MOD_N-GLC_2 | 411 | 413 | PF02516 | 0.533 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.563 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.454 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.667 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.619 |
MOD_NEK2_2 | 637 | 642 | PF00069 | 0.630 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.459 |
MOD_PIKK_1 | 654 | 660 | PF00454 | 0.558 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.643 |
MOD_PKA_1 | 609 | 615 | PF00069 | 0.560 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.491 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.561 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.577 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.609 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.659 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.560 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.633 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.532 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.422 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.627 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.584 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.630 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.435 |
MOD_Plk_4 | 637 | 643 | PF00069 | 0.669 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.564 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.751 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.638 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.677 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.516 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.706 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.668 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.622 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.545 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.563 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.531 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P315 | Leptomonas seymouri | 34% | 100% |
A0A3Q8I910 | Leishmania donovani | 75% | 100% |
A4HUV7 | Leishmania infantum | 75% | 100% |
E9ANJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 100% |
Q4QH34 | Leishmania major | 73% | 99% |