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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALT0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 291 | 295 | PF00656 | 0.466 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.529 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 368 | 370 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.710 |
CLV_PCSK_PC1ET2_1 | 368 | 370 | PF00082 | 0.568 |
CLV_PCSK_PC7_1 | 483 | 489 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.713 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.383 |
DEG_ODPH_VHL_1 | 352 | 364 | PF01847 | 0.422 |
DEG_SCF_FBW7_1 | 441 | 446 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 69 | 73 | PF00917 | 0.462 |
DOC_ANK_TNKS_1 | 232 | 239 | PF00023 | 0.451 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.685 |
DOC_CYCLIN_yCln2_LP_2 | 45 | 51 | PF00134 | 0.529 |
DOC_MAPK_gen_1 | 105 | 111 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 158 | 166 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.435 |
DOC_MAPK_MEF2A_6 | 188 | 196 | PF00069 | 0.517 |
DOC_MAPK_NFAT4_5 | 106 | 114 | PF00069 | 0.457 |
DOC_MAPK_NFAT4_5 | 189 | 197 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 499 | 506 | PF00149 | 0.532 |
DOC_PP2B_LxvP_1 | 164 | 167 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 45 | 48 | PF13499 | 0.481 |
DOC_PP2B_LxvP_1 | 491 | 494 | PF13499 | 0.491 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 241 | 250 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 334 | 339 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 392 | 400 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 66 | 70 | PF00244 | 0.778 |
LIG_Actin_WH2_2 | 333 | 351 | PF00022 | 0.494 |
LIG_AP2alpha_1 | 176 | 180 | PF02296 | 0.447 |
LIG_APCC_ABBA_1 | 173 | 178 | PF00400 | 0.598 |
LIG_APCC_ABBA_1 | 221 | 226 | PF00400 | 0.432 |
LIG_APCC_ABBA_1 | 473 | 478 | PF00400 | 0.474 |
LIG_BIR_III_4 | 301 | 305 | PF00653 | 0.603 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.732 |
LIG_BRCT_BRCA1_1 | 213 | 217 | PF00533 | 0.245 |
LIG_deltaCOP1_diTrp_1 | 128 | 137 | PF00928 | 0.628 |
LIG_deltaCOP1_diTrp_1 | 79 | 88 | PF00928 | 0.470 |
LIG_EVH1_2 | 360 | 364 | PF00568 | 0.464 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.728 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.314 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.701 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.710 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.586 |
LIG_Integrin_RGD_1 | 182 | 184 | PF01839 | 0.456 |
LIG_LIR_Gen_1 | 128 | 137 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 79 | 86 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.469 |
LIG_MYND_1 | 209 | 213 | PF01753 | 0.274 |
LIG_NRBOX | 191 | 197 | PF00104 | 0.511 |
LIG_NRP_CendR_1 | 504 | 506 | PF00754 | 0.545 |
LIG_Pex14_2 | 176 | 180 | PF04695 | 0.598 |
LIG_SH2_GRB2like | 453 | 456 | PF00017 | 0.503 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.584 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.322 |
LIG_SH2_SRC | 412 | 415 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.682 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.640 |
LIG_SH3_1 | 4 | 10 | PF00018 | 0.456 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.686 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.420 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.455 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.499 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.664 |
LIG_TRAF2_1 | 289 | 292 | PF00917 | 0.675 |
LIG_UBA3_1 | 194 | 200 | PF00899 | 0.367 |
MOD_CDK_SPK_2 | 36 | 41 | PF00069 | 0.463 |
MOD_CDK_SPK_2 | 429 | 434 | PF00069 | 0.659 |
MOD_CDK_SPK_2 | 53 | 58 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 36 | 43 | PF00069 | 0.465 |
MOD_CDK_SPxxK_3 | 494 | 501 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 51 | 58 | PF00069 | 0.599 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.636 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.357 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.512 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.634 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.683 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.709 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.601 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.545 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.746 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.647 |
MOD_Cter_Amidation | 103 | 106 | PF01082 | 0.453 |
MOD_DYRK1A_RPxSP_1 | 429 | 433 | PF00069 | 0.656 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.294 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.403 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.682 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.449 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.609 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.663 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.778 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.420 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.553 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.715 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.536 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.634 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.766 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.685 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.621 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.493 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.544 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.575 |
MOD_LATS_1 | 414 | 420 | PF00433 | 0.394 |
MOD_N-GLC_1 | 463 | 468 | PF02516 | 0.685 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.605 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.663 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.375 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.465 |
MOD_PK_1 | 334 | 340 | PF00069 | 0.255 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.710 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.415 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.677 |
MOD_PKB_1 | 41 | 49 | PF00069 | 0.621 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.644 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.431 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.475 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.588 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.638 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.476 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.536 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.655 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.675 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.522 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.745 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.716 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.653 |
TRG_DiLeu_BaLyEn_6 | 379 | 384 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 122 | 126 | PF00026 | 0.485 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 277 | 282 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 382 | 387 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 434 | 439 | PF00026 | 0.715 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P950 | Leptomonas seymouri | 40% | 91% |
A0A0N1ILX4 | Leptomonas seymouri | 25% | 100% |
A0A1X0NTZ8 | Trypanosomatidae | 27% | 100% |
A0A1X0NZT5 | Trypanosomatidae | 30% | 100% |
A0A3Q8IAB6 | Leishmania donovani | 24% | 93% |
A0A3R7KFA4 | Trypanosoma rangeli | 31% | 100% |
A0A3S5IRP3 | Trypanosoma rangeli | 28% | 100% |
A0A3S7X2J5 | Leishmania donovani | 90% | 94% |
A4H889 | Leishmania braziliensis | 25% | 100% |
A4HHF5 | Leishmania braziliensis | 80% | 100% |
A4HWL2 | Leishmania infantum | 24% | 93% |
A4I4K3 | Leishmania infantum | 90% | 94% |
C9ZL87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZXS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AE02 | Leishmania major | 90% | 100% |
E9AQB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4QF55 | Leishmania major | 25% | 100% |
V5B4N1 | Trypanosoma cruzi | 29% | 100% |
V5D9T1 | Trypanosoma cruzi | 30% | 100% |