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: E9AWY9
Term | Name | Level | Count |
---|---|---|---|
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0030656 | regulation of vitamin metabolic process | 5 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0062012 | regulation of small molecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0106064 | regulation of cobalamin metabolic process | 6 | 1 |
GO:1901401 | regulation of tetrapyrrole metabolic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016829 | lyase activity | 2 | 3 |
GO:0016830 | carbon-carbon lyase activity | 3 | 1 |
GO:0016833 | oxo-acid-lyase activity | 4 | 1 |
GO:0047777 | (S)-citramalyl-CoA lyase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.777 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.708 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.547 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.744 |
DOC_CDC14_PxL_1 | 167 | 175 | PF14671 | 0.590 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.557 |
DOC_CYCLIN_RxL_1 | 80 | 88 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 463 | 471 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 81 | 89 | PF00069 | 0.470 |
DOC_MAPK_RevD_3 | 178 | 192 | PF00069 | 0.384 |
DOC_PP1_RVXF_1 | 152 | 159 | PF00149 | 0.400 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.530 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.492 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.559 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.702 |
DOC_USP7_UBL2_3 | 479 | 483 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.636 |
LIG_14-3-3_CanoR_1 | 396 | 400 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 47 | 51 | PF00244 | 0.744 |
LIG_14-3-3_CterR_2 | 528 | 531 | PF00244 | 0.818 |
LIG_BIR_III_2 | 233 | 237 | PF00653 | 0.541 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.744 |
LIG_CaM_IQ_9 | 202 | 218 | PF13499 | 0.683 |
LIG_Clathr_ClatBox_1 | 404 | 408 | PF01394 | 0.546 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.561 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.760 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.491 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.555 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.734 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.464 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.524 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.560 |
LIG_LIR_Apic_2 | 284 | 288 | PF02991 | 0.492 |
LIG_LIR_Apic_2 | 383 | 389 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.603 |
LIG_LYPXL_yS_3 | 235 | 238 | PF13949 | 0.443 |
LIG_NRBOX | 257 | 263 | PF00104 | 0.530 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 425 | 429 | PF00017 | 0.597 |
LIG_SH2_PTP2 | 285 | 288 | PF00017 | 0.530 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.590 |
LIG_SH2_SRC | 285 | 288 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.653 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.546 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.384 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.750 |
LIG_SUMO_SIM_anti_2 | 297 | 304 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 178 | 185 | PF11976 | 0.512 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.590 |
LIG_UBA3_1 | 404 | 410 | PF00899 | 0.422 |
MOD_CDK_SPK_2 | 61 | 66 | PF00069 | 0.692 |
MOD_CDK_SPxK_1 | 520 | 526 | PF00069 | 0.825 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.425 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.741 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.534 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.728 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.484 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.470 |
MOD_GlcNHglycan | 323 | 327 | PF01048 | 0.432 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.630 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.619 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.771 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.519 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.655 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.443 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.697 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.777 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.674 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.743 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.614 |
MOD_N-GLC_1 | 513 | 518 | PF02516 | 0.533 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.351 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.618 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.779 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.459 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.380 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.597 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.607 |
MOD_NEK2_2 | 272 | 277 | PF00069 | 0.382 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.640 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.765 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.498 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.649 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.686 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.443 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.572 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.639 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.597 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.307 |
MOD_Plk_2-3 | 448 | 454 | PF00069 | 0.576 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.369 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.403 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.587 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.658 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.344 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.344 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.366 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.517 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.825 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 345 | 354 | PF00179 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.648 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 303 | 308 | PF01217 | 0.484 |
TRG_DiLeu_BaLyEn_6 | 400 | 405 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.784 |
TRG_ER_diArg_1 | 520 | 522 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 526 | 529 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.537 |
TRG_NLS_MonoExtC_3 | 190 | 195 | PF00514 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 397 | 401 | PF00026 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 403 | 408 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 83 | 88 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHZ0 | Leptomonas seymouri | 56% | 99% |
A0A1X0NVS5 | Trypanosomatidae | 31% | 100% |
A0A3S7WYJ5 | Leishmania donovani | 84% | 99% |
A4HDJ6 | Leishmania braziliensis | 70% | 99% |
C9ZWG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AH59 | Leishmania infantum | 84% | 99% |
Q4QAI7 | Leishmania major | 85% | 100% |
V5DBJ5 | Trypanosoma cruzi | 34% | 100% |