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: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0020023 | kinetoplast | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AE02
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.716 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 483 | 489 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.478 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.455 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.381 |
DEG_ODPH_VHL_1 | 352 | 364 | PF01847 | 0.413 |
DEG_SCF_FBW7_1 | 441 | 446 | PF00400 | 0.537 |
DEG_SCF_FBW7_1 | 61 | 68 | PF00400 | 0.517 |
DOC_ANK_TNKS_1 | 232 | 239 | PF00023 | 0.606 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.684 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.557 |
DOC_CKS1_1 | 62 | 67 | PF01111 | 0.487 |
DOC_CYCLIN_RxL_1 | 154 | 162 | PF00134 | 0.419 |
DOC_MAPK_gen_1 | 105 | 111 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 157 | 166 | PF00069 | 0.651 |
DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.520 |
DOC_MAPK_NFAT4_5 | 106 | 114 | PF00069 | 0.447 |
DOC_MAPK_NFAT4_5 | 189 | 197 | PF00069 | 0.520 |
DOC_PP1_RVXF_1 | 499 | 506 | PF00149 | 0.537 |
DOC_PP2B_LxvP_1 | 164 | 167 | PF13499 | 0.543 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.518 |
DOC_USP7_UBL2_3 | 157 | 161 | PF12436 | 0.417 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 241 | 250 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 33 | 40 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 334 | 341 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 392 | 400 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 429 | 436 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.788 |
LIG_Actin_WH2_2 | 333 | 351 | PF00022 | 0.502 |
LIG_AP2alpha_1 | 176 | 180 | PF02296 | 0.486 |
LIG_APCC_ABBA_1 | 173 | 178 | PF00400 | 0.634 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.510 |
LIG_APCC_ABBA_1 | 473 | 478 | PF00400 | 0.470 |
LIG_BIR_III_4 | 301 | 305 | PF00653 | 0.588 |
LIG_BRCT_BRCA1_1 | 501 | 505 | PF00533 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 128 | 137 | PF00928 | 0.614 |
LIG_deltaCOP1_diTrp_1 | 79 | 88 | PF00928 | 0.466 |
LIG_EVH1_2 | 10 | 14 | PF00568 | 0.525 |
LIG_EVH1_2 | 213 | 217 | PF00568 | 0.337 |
LIG_EVH1_2 | 360 | 364 | PF00568 | 0.456 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.708 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.711 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.822 |
LIG_Integrin_RGD_1 | 182 | 184 | PF01839 | 0.464 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 79 | 86 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.467 |
LIG_NRBOX | 191 | 197 | PF00104 | 0.514 |
LIG_NRP_CendR_1 | 504 | 506 | PF00754 | 0.544 |
LIG_PCNA_yPIPBox_3 | 277 | 287 | PF02747 | 0.336 |
LIG_Pex14_2 | 176 | 180 | PF04695 | 0.639 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.596 |
LIG_SH2_SRC | 412 | 415 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.690 |
LIG_SH3_1 | 488 | 494 | PF00018 | 0.533 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.691 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.548 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.306 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.701 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.589 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.756 |
LIG_SH3_CIN85_PxpxPR_1 | 61 | 66 | PF14604 | 0.564 |
LIG_SUMO_SIM_anti_2 | 282 | 289 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 282 | 289 | PF11976 | 0.426 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.709 |
LIG_UBA3_1 | 194 | 200 | PF00899 | 0.368 |
LIG_WW_3 | 9 | 13 | PF00397 | 0.473 |
MOD_CDK_SPK_2 | 53 | 58 | PF00069 | 0.611 |
MOD_CDK_SPK_2 | 61 | 66 | PF00069 | 0.558 |
MOD_CDK_SPxxK_3 | 150 | 157 | PF00069 | 0.427 |
MOD_CDK_SPxxK_3 | 494 | 501 | PF00069 | 0.549 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.611 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.664 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.371 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.541 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.701 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.623 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.589 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.743 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.658 |
MOD_Cter_Amidation | 103 | 106 | PF01082 | 0.466 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.438 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.667 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.488 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.498 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.549 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.453 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.559 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.679 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.598 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.639 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.724 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.686 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.592 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.621 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.706 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.682 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.617 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.718 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.713 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.390 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.738 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.435 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.684 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.688 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.544 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.547 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.463 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.590 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.641 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.560 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.541 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.687 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.715 |
MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.609 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.519 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.531 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.656 |
TRG_DiLeu_BaLyEn_6 | 379 | 384 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 122 | 126 | PF00026 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 382 | 387 | PF00026 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 434 | 439 | PF00026 | 0.758 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P950 | Leptomonas seymouri | 39% | 91% |
A0A0N1ILX4 | Leptomonas seymouri | 25% | 100% |
A0A0S4JKE9 | Bodo saltans | 27% | 100% |
A0A1X0NTZ8 | Trypanosomatidae | 27% | 100% |
A0A1X0NZT5 | Trypanosomatidae | 31% | 100% |
A0A3Q8IAB6 | Leishmania donovani | 25% | 93% |
A0A3R7KFA4 | Trypanosoma rangeli | 31% | 100% |
A0A3S5IRP3 | Trypanosoma rangeli | 27% | 100% |
A0A3S7X2J5 | Leishmania donovani | 94% | 94% |
A4H889 | Leishmania braziliensis | 25% | 100% |
A4HHF5 | Leishmania braziliensis | 81% | 100% |
A4HWL2 | Leishmania infantum | 25% | 93% |
A4I4K3 | Leishmania infantum | 94% | 94% |
C9ZL87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZXS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9ALT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9AQB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4QF55 | Leishmania major | 25% | 95% |
V5B4N1 | Trypanosoma cruzi | 27% | 100% |
V5D9T1 | Trypanosoma cruzi | 30% | 100% |