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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q0K1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.678 |
CLV_C14_Caspase3-7 | 238 | 242 | PF00656 | 0.498 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.762 |
CLV_PCSK_FUR_1 | 316 | 320 | PF00082 | 0.529 |
CLV_PCSK_FUR_1 | 475 | 479 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.791 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 23 | 29 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.566 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.658 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.616 |
DEG_SPOP_SBC_1 | 156 | 160 | PF00917 | 0.644 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.347 |
DEG_SPOP_SBC_1 | 523 | 527 | PF00917 | 0.557 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.559 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.735 |
DOC_CYCLIN_RxL_1 | 227 | 237 | PF00134 | 0.571 |
DOC_CYCLIN_yCln2_LP_2 | 152 | 155 | PF00134 | 0.705 |
DOC_CYCLIN_yCln2_LP_2 | 283 | 289 | PF00134 | 0.499 |
DOC_CYCLIN_yCln2_LP_2 | 427 | 433 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.753 |
DOC_MAPK_gen_1 | 447 | 454 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 503 | 513 | PF00069 | 0.415 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.701 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.492 |
DOC_PP4_FxxP_1 | 198 | 201 | PF00568 | 0.456 |
DOC_PP4_FxxP_1 | 9 | 12 | PF00568 | 0.538 |
DOC_SPAK_OSR1_1 | 172 | 176 | PF12202 | 0.713 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.707 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 191 | 198 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 246 | 252 | PF00244 | 0.730 |
LIG_14-3-3_CanoR_1 | 327 | 332 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 360 | 364 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 365 | 373 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 447 | 455 | PF00244 | 0.438 |
LIG_Actin_WH2_2 | 490 | 505 | PF00022 | 0.513 |
LIG_BIR_III_2 | 34 | 38 | PF00653 | 0.676 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 518 | 522 | PF00533 | 0.499 |
LIG_CSL_BTD_1 | 9 | 12 | PF09270 | 0.733 |
LIG_DLG_GKlike_1 | 376 | 384 | PF00625 | 0.404 |
LIG_EH1_1 | 328 | 336 | PF00400 | 0.522 |
LIG_eIF4E_1 | 329 | 335 | PF01652 | 0.432 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.493 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.613 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.484 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.605 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.719 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.554 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.489 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.571 |
LIG_LIR_Apic_2 | 197 | 201 | PF02991 | 0.369 |
LIG_NRBOX | 333 | 339 | PF00104 | 0.391 |
LIG_Pex14_1 | 10 | 14 | PF04695 | 0.617 |
LIG_RPA_C_Fungi | 24 | 36 | PF08784 | 0.749 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.520 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.512 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 551 | 555 | PF00017 | 0.582 |
LIG_SH2_SRC | 551 | 554 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.533 |
LIG_SH3_2 | 183 | 188 | PF14604 | 0.698 |
LIG_SH3_2 | 63 | 68 | PF14604 | 0.706 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.519 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.709 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.703 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.519 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.715 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.764 |
LIG_SUMO_SIM_par_1 | 299 | 309 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 456 | 462 | PF11976 | 0.461 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.541 |
LIG_TYR_ITIM | 321 | 326 | PF00017 | 0.503 |
LIG_WW_3 | 185 | 189 | PF00397 | 0.767 |
MOD_CDK_SPK_2 | 8 | 13 | PF00069 | 0.734 |
MOD_CDK_SPxK_1 | 2 | 8 | PF00069 | 0.662 |
MOD_CDK_SPxxK_3 | 163 | 170 | PF00069 | 0.678 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.669 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.628 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.738 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.747 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.680 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.826 |
MOD_Cter_Amidation | 25 | 28 | PF01082 | 0.784 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.589 |
MOD_Cter_Amidation | 475 | 478 | PF01082 | 0.503 |
MOD_DYRK1A_RPxSP_1 | 387 | 391 | PF00069 | 0.654 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.694 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.763 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.711 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.611 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.699 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.530 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.728 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.511 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.705 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.722 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.701 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.741 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.671 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.724 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.554 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.527 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.507 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.476 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.719 |
MOD_LATS_1 | 374 | 380 | PF00433 | 0.502 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.530 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.558 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.471 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.403 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.540 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.488 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.435 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.489 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.513 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.540 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.701 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.555 |
MOD_PK_1 | 327 | 333 | PF00069 | 0.467 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.642 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.506 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.739 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.452 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.692 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.468 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.639 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.537 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.532 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.645 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.679 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.651 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.716 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.655 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.679 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.743 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.698 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.772 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.660 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.722 |
TRG_DiLeu_BaEn_1 | 216 | 221 | PF01217 | 0.499 |
TRG_DiLeu_BaEn_2 | 488 | 494 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.742 |
TRG_ER_diArg_1 | 316 | 319 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 475 | 478 | PF00400 | 0.503 |
TRG_NLS_MonoExtC_3 | 26 | 31 | PF00514 | 0.789 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMS8 | Leptomonas seymouri | 46% | 95% |
A0A1X0P1C1 | Trypanosomatidae | 28% | 100% |
A0A3Q8IJU5 | Leishmania donovani | 90% | 100% |
A0A3R7M711 | Trypanosoma rangeli | 29% | 100% |
A4HQ76 | Leishmania braziliensis | 72% | 100% |
A4IDX4 | Leishmania infantum | 90% | 100% |
D0A438 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ATZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |