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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4Q3V6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 479 | 483 | PF00656 | 0.674 |
CLV_NRD_NRD_1 | 1 | 3 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.352 |
CLV_PCSK_FUR_1 | 190 | 194 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 364 | 372 | PF00400 | 0.488 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.597 |
DEG_SCF_FBW7_1 | 310 | 315 | PF00400 | 0.598 |
DEG_SPOP_SBC_1 | 304 | 308 | PF00917 | 0.608 |
DEG_SPOP_SBC_1 | 312 | 316 | PF00917 | 0.504 |
DEG_SPOP_SBC_1 | 337 | 341 | PF00917 | 0.610 |
DOC_ANK_TNKS_1 | 469 | 476 | PF00023 | 0.452 |
DOC_ANK_TNKS_1 | 483 | 490 | PF00023 | 0.399 |
DOC_CYCLIN_RxL_1 | 190 | 197 | PF00134 | 0.524 |
DOC_CYCLIN_RxL_1 | 392 | 401 | PF00134 | 0.374 |
DOC_CYCLIN_RxL_1 | 46 | 55 | PF00134 | 0.495 |
DOC_CYCLIN_yCln2_LP_2 | 519 | 525 | PF00134 | 0.493 |
DOC_MAPK_gen_1 | 2 | 9 | PF00069 | 0.536 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.545 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 136 | 140 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 2 | 8 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 324 | 332 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 395 | 400 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.671 |
LIG_AP2alpha_2 | 83 | 85 | PF02296 | 0.551 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.679 |
LIG_BRCT_BRCA1_2 | 69 | 75 | PF00533 | 0.588 |
LIG_deltaCOP1_diTrp_1 | 127 | 131 | PF00928 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 411 | 418 | PF00928 | 0.534 |
LIG_EVH1_2 | 288 | 292 | PF00568 | 0.602 |
LIG_EVH1_2 | 445 | 449 | PF00568 | 0.456 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.675 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.714 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.434 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.345 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.387 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.596 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.410 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.825 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.499 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.578 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.582 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.642 |
LIG_Integrin_RGD_1 | 234 | 236 | PF01839 | 0.615 |
LIG_LIR_Apic_2 | 89 | 94 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 127 | 134 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 38 | 44 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 415 | 425 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.704 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.488 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.507 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.573 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.637 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.661 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.486 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.546 |
LIG_SUMO_SIM_par_1 | 403 | 408 | PF11976 | 0.516 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.531 |
LIG_WRC_WIRS_1 | 203 | 208 | PF05994 | 0.405 |
LIG_WW_3 | 444 | 448 | PF00397 | 0.478 |
MOD_CDC14_SPxK_1 | 343 | 346 | PF00782 | 0.537 |
MOD_CDK_SPxK_1 | 340 | 346 | PF00069 | 0.541 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.402 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.620 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.757 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.570 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.773 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.605 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.536 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.573 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.559 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.709 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.488 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.593 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.671 |
MOD_DYRK1A_RPxSP_1 | 77 | 81 | PF00069 | 0.630 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.652 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.579 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.631 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.625 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.705 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.698 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.709 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.795 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.551 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.626 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.658 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.402 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.560 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.747 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.567 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.754 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.656 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.751 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.578 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.511 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.541 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.678 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.558 |
MOD_N-GLC_1 | 198 | 203 | PF02516 | 0.566 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.697 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.545 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.768 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.442 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.637 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.631 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.502 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.520 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.762 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.530 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.598 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.506 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.745 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.582 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.610 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.637 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.669 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.678 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.569 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.535 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.431 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.612 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.610 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.402 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.350 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.596 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.489 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.404 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.448 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.720 |
MOD_ProDKin_1 | 340 | 346 | PF00069 | 0.739 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 191 | 196 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.600 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 510 | 515 | PF00026 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 77 | 82 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF55 | Leptomonas seymouri | 52% | 98% |
A0A3S7X722 | Leishmania donovani | 88% | 100% |
A4HLU4 | Leishmania braziliensis | 70% | 100% |
D0A684 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AHP9 | Leishmania infantum | 89% | 100% |
E9B470 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5B8P3 | Trypanosoma cruzi | 33% | 100% |