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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019752 | carboxylic acid metabolic process | 5 | 10 |
GO:0043436 | oxoacid metabolic process | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044281 | small molecule metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0016829 | lyase activity | 2 | 10 |
GO:0016830 | carbon-carbon lyase activity | 3 | 10 |
GO:0019842 | vitamin binding | 3 | 10 |
GO:0030170 | pyridoxal phosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0070279 | vitamin B6 binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0016831 | carboxy-lyase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.412 |
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.639 |
CLV_MEL_PAP_1 | 379 | 385 | PF00089 | 0.546 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.670 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.560 |
DEG_APCC_DBOX_1 | 390 | 398 | PF00400 | 0.531 |
DEG_COP1_1 | 261 | 272 | PF00400 | 0.432 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.568 |
DEG_SCF_FBW7_1 | 54 | 59 | PF00400 | 0.580 |
DOC_CKS1_1 | 323 | 328 | PF01111 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.465 |
DOC_MAPK_MEF2A_6 | 482 | 491 | PF00069 | 0.571 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 510 | 513 | PF13499 | 0.568 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 135 | 141 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 316 | 321 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 543 | 548 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 8 | 16 | PF00244 | 0.654 |
LIG_deltaCOP1_diTrp_1 | 343 | 347 | PF00928 | 0.533 |
LIG_Dynein_DLC8_1 | 133 | 139 | PF01221 | 0.375 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.427 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.542 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.519 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.508 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.467 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.465 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.579 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.503 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.644 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.401 |
LIG_Integrin_RGD_1 | 398 | 400 | PF01839 | 0.546 |
LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 250 | 260 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 73 | 82 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 505 | 509 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 73 | 78 | PF02991 | 0.504 |
LIG_LYPXL_S_1 | 188 | 192 | PF13949 | 0.269 |
LIG_LYPXL_yS_3 | 189 | 192 | PF13949 | 0.269 |
LIG_RPA_C_Fungi | 427 | 439 | PF08784 | 0.511 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.551 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 133 | 136 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.336 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.550 |
LIG_SH3_2 | 244 | 249 | PF14604 | 0.333 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.713 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.596 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.476 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.705 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.550 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.724 |
LIG_SH3_4 | 364 | 371 | PF00018 | 0.450 |
LIG_SUMO_SIM_anti_2 | 206 | 213 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 375 | 381 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 508 | 516 | PF11976 | 0.596 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.400 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.531 |
LIG_TYR_ITIM | 131 | 136 | PF00017 | 0.331 |
LIG_TYR_ITIM | 276 | 281 | PF00017 | 0.601 |
LIG_WRC_WIRS_1 | 194 | 199 | PF05994 | 0.385 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.613 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.385 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.557 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.570 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.641 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.534 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.577 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.440 |
MOD_DYRK1A_RPxSP_1 | 52 | 56 | PF00069 | 0.587 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.747 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.505 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.384 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.546 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.596 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.679 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.695 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.589 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.618 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.397 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.409 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.481 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.617 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.548 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.418 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.578 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.581 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.365 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.179 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.383 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.501 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.499 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.685 |
MOD_PKB_1 | 541 | 549 | PF00069 | 0.481 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.516 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.601 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.571 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.390 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.686 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.560 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.605 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.398 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.646 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.575 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.644 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.665 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.757 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.675 |
MOD_SUMO_rev_2 | 519 | 527 | PF00179 | 0.501 |
TRG_DiLeu_BaEn_1 | 516 | 521 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 505 | 510 | PF01217 | 0.657 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.519 |
TRG_NES_CRM1_1 | 213 | 225 | PF08389 | 0.184 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL2 | Leptomonas seymouri | 45% | 77% |
A0A1X0P0L1 | Trypanosomatidae | 27% | 83% |
A0A3Q8IDL2 | Leishmania donovani | 88% | 100% |
A0A3R7K963 | Trypanosoma rangeli | 34% | 100% |
A4H8G7 | Leishmania braziliensis | 75% | 100% |
A4HWU0 | Leishmania infantum | 88% | 100% |
C9ZW41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 94% |
Q4QEX8 | Leishmania major | 87% | 100% |