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: A4HDJ6
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 | 9 |
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 | 451 | 455 | PF00656 | 0.438 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.395 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 444 | 446 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.499 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.599 |
DOC_CDC14_PxL_1 | 172 | 180 | PF14671 | 0.495 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.555 |
DOC_CYCLIN_RxL_1 | 80 | 88 | PF00134 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 330 | 336 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 413 | 419 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 464 | 472 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 157 | 164 | PF00149 | 0.377 |
DOC_PP1_RVXF_1 | 81 | 88 | PF00149 | 0.360 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.464 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.473 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.660 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.572 |
LIG_14-3-3_CanoR_1 | 2 | 12 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 36 | 46 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 397 | 401 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 47 | 57 | PF00244 | 0.686 |
LIG_14-3-3_CterR_2 | 529 | 532 | PF00244 | 0.692 |
LIG_APCC_ABBA_1 | 89 | 94 | PF00400 | 0.483 |
LIG_BRCT_BRCA1_1 | 159 | 163 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.545 |
LIG_CaM_IQ_9 | 207 | 223 | PF13499 | 0.516 |
LIG_CaM_NSCaTE_8 | 14 | 21 | PF13499 | 0.440 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.699 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.516 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.473 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.524 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.511 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.355 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.471 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.449 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.499 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.484 |
LIG_LIR_Apic_2 | 286 | 290 | PF02991 | 0.451 |
LIG_LIR_Apic_2 | 384 | 390 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.620 |
LIG_LYPXL_yS_3 | 237 | 240 | PF13949 | 0.377 |
LIG_MYND_1 | 154 | 158 | PF01753 | 0.522 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.473 |
LIG_SH2_NCK_1 | 249 | 253 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 426 | 430 | PF00017 | 0.457 |
LIG_SH2_PTP2 | 287 | 290 | PF00017 | 0.473 |
LIG_SH2_SRC | 249 | 252 | PF00017 | 0.495 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.449 |
LIG_SH2_SRC | 316 | 319 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.501 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.483 |
LIG_SUMO_SIM_anti_2 | 21 | 26 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 257 | 262 | PF11976 | 0.425 |
LIG_SUMO_SIM_anti_2 | 299 | 306 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.476 |
LIG_SUMO_SIM_par_1 | 253 | 259 | PF11976 | 0.387 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.543 |
LIG_TRAF2_1 | 399 | 402 | PF00917 | 0.525 |
MOD_CDC14_SPxK_1 | 64 | 67 | PF00782 | 0.503 |
MOD_CDK_SPK_2 | 42 | 47 | PF00069 | 0.549 |
MOD_CDK_SPxK_1 | 42 | 48 | PF00069 | 0.554 |
MOD_CDK_SPxK_1 | 521 | 527 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 61 | 67 | PF00069 | 0.469 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.527 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.661 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.377 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.273 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.692 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.696 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.451 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.474 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.349 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.406 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.475 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.480 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.428 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.283 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.717 |
MOD_GlcNHglycan | 493 | 497 | PF01048 | 0.524 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.800 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.659 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.692 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.708 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.209 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.377 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.286 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.275 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.654 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.587 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.763 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.591 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.462 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.624 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.289 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.293 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.363 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.302 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.715 |
MOD_NEK2_2 | 117 | 122 | PF00069 | 0.443 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.471 |
MOD_NEK2_2 | 274 | 279 | PF00069 | 0.290 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.328 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.290 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.349 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.461 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.563 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.377 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.471 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.590 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.650 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.545 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.447 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.635 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.366 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.197 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.377 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.347 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.483 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.653 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.283 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.661 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.283 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.665 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.431 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.680 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.574 |
MOD_SUMO_rev_2 | 345 | 355 | PF00179 | 0.273 |
TRG_DiLeu_BaEn_1 | 259 | 264 | PF01217 | 0.207 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.644 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.220 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 404 | 406 | PF00400 | 0.377 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 398 | 402 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 83 | 88 | PF00026 | 0.552 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHZ0 | Leptomonas seymouri | 56% | 99% |
A0A1X0NVS5 | Trypanosomatidae | 31% | 100% |
A0A3S7WYJ5 | Leishmania donovani | 74% | 99% |
E9AH59 | Leishmania infantum | 74% | 99% |
E9AWY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4QAI7 | Leishmania major | 74% | 100% |
V5DBJ5 | Trypanosoma cruzi | 35% | 100% |