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: E9AJM4
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 | 159 | 163 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.760 |
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.572 |
CLV_C14_Caspase3-7 | 498 | 502 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 555 | 559 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.764 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 541 | 543 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.507 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.750 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.542 |
DEG_APCC_DBOX_1 | 67 | 75 | PF00400 | 0.601 |
DEG_SPOP_SBC_1 | 82 | 86 | PF00917 | 0.588 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 377 | 387 | PF00134 | 0.545 |
DOC_MAPK_gen_1 | 15 | 22 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 377 | 385 | PF00069 | 0.590 |
DOC_PP1_RVXF_1 | 510 | 517 | PF00149 | 0.395 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.598 |
DOC_PP2B_LxvP_1 | 444 | 447 | PF13499 | 0.371 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.659 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 133 | 141 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 26 | 31 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 284 | 291 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 362 | 366 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 426 | 431 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 461 | 468 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 563 | 572 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 67 | 83 | PF00022 | 0.513 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.495 |
LIG_BRCT_BRCA1_1 | 148 | 152 | PF00533 | 0.547 |
LIG_EH_1 | 179 | 183 | PF12763 | 0.274 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.597 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.609 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.538 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.316 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.344 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.447 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.589 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.499 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.394 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.542 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.454 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.580 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.613 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.675 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.496 |
LIG_LIR_Gen_1 | 296 | 303 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 341 | 349 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 341 | 346 | PF02991 | 0.420 |
LIG_MLH1_MIPbox_1 | 148 | 152 | PF16413 | 0.547 |
LIG_NRBOX | 407 | 413 | PF00104 | 0.659 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.512 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.538 |
LIG_SH2_NCK_1 | 224 | 228 | PF00017 | 0.482 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.484 |
LIG_SH2_SRC | 349 | 352 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 506 | 510 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 539 | 543 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.481 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.523 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.530 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.633 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.535 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.565 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.368 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.664 |
LIG_SH3_3 | 507 | 513 | PF00018 | 0.475 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.705 |
LIG_SUMO_SIM_anti_2 | 350 | 357 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 440 | 447 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 321 | 326 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 354 | 360 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 568 | 573 | PF11976 | 0.483 |
LIG_TRAF2_1 | 463 | 466 | PF00917 | 0.525 |
LIG_TRFH_1 | 182 | 186 | PF08558 | 0.512 |
LIG_TYR_ITSM | 339 | 346 | PF00017 | 0.492 |
LIG_WW_3 | 560 | 564 | PF00397 | 0.508 |
MOD_CDC14_SPxK_1 | 308 | 311 | PF00782 | 0.315 |
MOD_CDK_SPK_2 | 29 | 34 | PF00069 | 0.403 |
MOD_CDK_SPxK_1 | 305 | 311 | PF00069 | 0.319 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.500 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.704 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.479 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.749 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.432 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.666 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.486 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.737 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.578 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.519 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.386 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.526 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.498 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.501 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.565 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.652 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.665 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.452 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.742 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.472 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.337 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.587 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.633 |
MOD_GlcNHglycan | 527 | 531 | PF01048 | 0.609 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.760 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.746 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.728 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.570 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.578 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.496 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.560 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.457 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.605 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.481 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.398 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.499 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.529 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.725 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.578 |
MOD_LATS_1 | 195 | 201 | PF00433 | 0.255 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.664 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.579 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.619 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.610 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.409 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.179 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.495 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.546 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.457 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.638 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.496 |
MOD_NEK2_2 | 534 | 539 | PF00069 | 0.496 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.517 |
MOD_PK_1 | 26 | 32 | PF00069 | 0.579 |
MOD_PKA_1 | 563 | 569 | PF00069 | 0.496 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.602 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.661 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.470 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.429 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.593 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.501 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.671 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.484 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.662 |
MOD_Plk_1 | 500 | 506 | PF00069 | 0.497 |
MOD_Plk_2-3 | 351 | 357 | PF00069 | 0.527 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.584 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.662 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.543 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.497 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.407 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.585 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.479 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.657 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.512 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.578 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.467 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.509 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.502 |
MOD_SUMO_rev_2 | 418 | 427 | PF00179 | 0.598 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.398 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 541 | 543 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 562 | 564 | PF00400 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHU3 | Leptomonas seymouri | 49% | 100% |
A0A1X0NJL9 | Trypanosomatidae | 29% | 100% |
A0A3R7NH89 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WNM2 | Leishmania donovani | 88% | 100% |
A4H3F3 | Leishmania braziliensis | 73% | 100% |
A4HRQ7 | Leishmania infantum | 87% | 100% |
C9ZJ47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ACD6 | Leishmania major | 85% | 100% |
V5BER3 | Trypanosoma cruzi | 30% | 100% |