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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H3F3
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 1 |
GO:0006448 | regulation of translational elongation | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0017182 | peptidyl-diphthamide metabolic process | 7 | 1 |
GO:0017183 | peptidyl-diphthamide biosynthetic process from peptidyl-histidine | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018202 | peptidyl-histidine modification | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 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:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1900247 | regulation of cytoplasmic translational elongation | 8 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 1 |
GO:0061685 | diphthine methylesterase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 257 | 261 | PF00656 | 0.785 |
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.750 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.528 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.405 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.754 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.551 |
DEG_APCC_DBOX_1 | 58 | 66 | PF00400 | 0.582 |
DEG_SCF_TRCP1_1 | 378 | 384 | PF00400 | 0.689 |
DOC_CDC14_PxL_1 | 30 | 38 | PF14671 | 0.368 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.458 |
DOC_CYCLIN_RxL_1 | 368 | 378 | PF00134 | 0.563 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 37 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 368 | 376 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 58 | 64 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 501 | 508 | PF00149 | 0.393 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.582 |
DOC_PP2B_LxvP_1 | 435 | 438 | PF13499 | 0.385 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.713 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 124 | 133 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 323 | 333 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 411 | 418 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 452 | 459 | PF00244 | 0.593 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.314 |
LIG_DLG_GKlike_1 | 58 | 65 | PF00625 | 0.336 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.593 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.552 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.317 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.457 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.531 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.407 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.532 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.454 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.698 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.340 |
LIG_FHA_2 | 337 | 343 | PF00498 | 0.282 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.607 |
LIG_LIR_Gen_1 | 287 | 294 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 332 | 340 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.431 |
LIG_MLH1_MIPbox_1 | 139 | 143 | PF16413 | 0.553 |
LIG_NRBOX | 398 | 404 | PF00104 | 0.683 |
LIG_REV1ctd_RIR_1 | 140 | 147 | PF16727 | 0.376 |
LIG_SH2_CRK | 104 | 108 | PF00017 | 0.497 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.540 |
LIG_SH2_NCK_1 | 215 | 219 | PF00017 | 0.488 |
LIG_SH2_SRC | 215 | 218 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 497 | 501 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 530 | 534 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.480 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.525 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.532 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.513 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.606 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.554 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.497 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.489 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.685 |
LIG_SUMO_SIM_anti_2 | 342 | 348 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 310 | 317 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 345 | 351 | PF11976 | 0.532 |
LIG_TRAF2_1 | 454 | 457 | PF00917 | 0.537 |
LIG_TYR_ITSM | 330 | 337 | PF00017 | 0.504 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.456 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.412 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.482 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.715 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.490 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.636 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.748 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.391 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.543 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.631 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.498 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.473 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.495 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.657 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.448 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.582 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.761 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.536 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.339 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.699 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.655 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.723 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.604 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.732 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.591 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.548 |
MOD_GlcNHglycan | 518 | 522 | PF01048 | 0.612 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.564 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.612 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.517 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.504 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.404 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.669 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.645 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.439 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.532 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.506 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.686 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.660 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.616 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.414 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.179 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.283 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.498 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.554 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.438 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.669 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.659 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.507 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.545 |
MOD_NEK2_2 | 525 | 530 | PF00069 | 0.496 |
MOD_OFUCOSY | 419 | 426 | PF10250 | 0.455 |
MOD_PK_1 | 17 | 23 | PF00069 | 0.554 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.344 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.608 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.663 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.445 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.610 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.609 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.344 |
MOD_PKB_1 | 306 | 314 | PF00069 | 0.321 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.684 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.533 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.587 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.684 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.407 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.587 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.498 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.493 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.652 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.483 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.525 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.561 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.564 |
MOD_SUMO_rev_2 | 413 | 418 | PF00179 | 0.645 |
MOD_SUMO_rev_2 | 8 | 18 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 183 | 188 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHU3 | Leptomonas seymouri | 50% | 100% |
A0A1X0NJL9 | Trypanosomatidae | 29% | 100% |
A0A3R7NH89 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WNM2 | Leishmania donovani | 75% | 96% |
A4HRQ7 | Leishmania infantum | 75% | 96% |
C9ZJ47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9ACD6 | Leishmania major | 72% | 100% |
E9AJM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 73% | 94% |
V5BER3 | Trypanosoma cruzi | 28% | 100% |