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: Q4QCG4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.707 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.657 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 464 | 466 | PF00082 | 0.774 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.785 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.422 |
DEG_SCF_FBW7_1 | 148 | 154 | PF00400 | 0.531 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.726 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.541 |
DOC_CDC14_PxL_1 | 192 | 200 | PF14671 | 0.557 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.531 |
DOC_CKS1_1 | 531 | 536 | PF01111 | 0.801 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 444 | 450 | PF00134 | 0.562 |
DOC_MAPK_gen_1 | 142 | 148 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.694 |
DOC_MAPK_gen_1 | 462 | 471 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 414 | 423 | PF00069 | 0.779 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.501 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.595 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 530 | 535 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 344 | 348 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 465 | 469 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 499 | 504 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.755 |
LIG_Actin_WH2_2 | 127 | 144 | PF00022 | 0.570 |
LIG_APCC_ABBA_1 | 248 | 253 | PF00400 | 0.461 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.740 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.669 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.642 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.500 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.528 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.662 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.462 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.581 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.611 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.720 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.454 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.591 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.709 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.534 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.757 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 467 | 476 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 467 | 471 | PF02991 | 0.550 |
LIG_MYND_1 | 196 | 200 | PF01753 | 0.553 |
LIG_MYND_1 | 451 | 455 | PF01753 | 0.628 |
LIG_MYND_3 | 134 | 138 | PF01753 | 0.533 |
LIG_NRBOX | 176 | 182 | PF00104 | 0.462 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.655 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.586 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.609 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.529 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.547 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.417 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.559 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.730 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.601 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.697 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.693 |
LIG_SH3_3 | 509 | 515 | PF00018 | 0.489 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.722 |
LIG_SH3_3 | 535 | 541 | PF00018 | 0.697 |
LIG_SH3_3 | 542 | 548 | PF00018 | 0.647 |
LIG_Sin3_3 | 456 | 463 | PF02671 | 0.761 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.608 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.475 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.643 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.599 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.516 |
LIG_UBA3_1 | 133 | 142 | PF00899 | 0.520 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.722 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.650 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.685 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.690 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.772 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.488 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.424 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.601 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.579 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.540 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.531 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.743 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.746 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.655 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.723 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.497 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.684 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.746 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.538 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.737 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.462 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.655 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.651 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.606 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.658 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.772 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.691 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.731 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.703 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.401 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.366 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.677 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.490 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.291 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.562 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.698 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.709 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.726 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.549 |
MOD_PK_1 | 415 | 421 | PF00069 | 0.748 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.753 |
MOD_PKA_1 | 414 | 420 | PF00069 | 0.737 |
MOD_PKA_1 | 464 | 470 | PF00069 | 0.695 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.536 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.676 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.638 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.609 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.490 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.567 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.440 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.720 |
MOD_ProDKin_1 | 530 | 536 | PF00069 | 0.808 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.750 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.723 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.716 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.749 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.510 |
TRG_NLS_MonoExtN_4 | 254 | 261 | PF00514 | 0.525 |
TRG_NLS_MonoExtN_4 | 462 | 468 | PF00514 | 0.771 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAT9 | Leptomonas seymouri | 56% | 95% |
A0A3Q8IAT2 | Leishmania donovani | 90% | 100% |
A0A422NBI2 | Trypanosoma rangeli | 26% | 100% |
A4HBP8 | Leishmania braziliensis | 73% | 100% |
A4HZ50 | Leishmania infantum | 90% | 100% |
D0A1Q2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AV18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5BKP0 | Trypanosoma cruzi | 27% | 100% |