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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACD6
Term | Name | Level | Count |
---|---|---|---|
GO:0006417 | regulation of translation | 6 | 2 |
GO:0006448 | regulation of translational elongation | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0017182 | peptidyl-diphthamide metabolic process | 7 | 2 |
GO:0017183 | peptidyl-diphthamide biosynthetic process from peptidyl-histidine | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018202 | peptidyl-histidine modification | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0034248 | regulation of amide metabolic process | 5 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051246 | regulation of protein metabolic process | 5 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:1900247 | regulation of cytoplasmic translational elongation | 8 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 2 |
GO:0061685 | diphthine methylesterase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.771 |
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.750 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 511 | 515 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 528 | 532 | PF00656 | 0.384 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.447 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 438 | 440 | PF00082 | 0.746 |
CLV_PCSK_PC7_1 | 434 | 440 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.531 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.592 |
DEG_SCF_TRCP1_1 | 400 | 406 | PF00400 | 0.655 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.596 |
DOC_CYCLIN_RxL_1 | 390 | 400 | PF00134 | 0.531 |
DOC_MAPK_gen_1 | 390 | 398 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 77 | 85 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 77 | 85 | PF00069 | 0.513 |
DOC_PP2B_LxvP_1 | 457 | 460 | PF13499 | 0.375 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.538 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.649 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 145 | 153 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 27 | 33 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 297 | 304 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 38 | 43 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 439 | 444 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 474 | 481 | PF00244 | 0.571 |
LIG_Actin_WH2_2 | 79 | 95 | PF00022 | 0.504 |
LIG_AP2alpha_2 | 192 | 194 | PF02296 | 0.434 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 405 | 409 | PF00533 | 0.490 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.567 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.581 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.522 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.311 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.340 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.431 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.585 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.563 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.481 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.380 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.530 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.647 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.591 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.667 |
LIG_LIR_Gen_1 | 309 | 318 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 354 | 362 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 354 | 359 | PF02991 | 0.408 |
LIG_MLH1_MIPbox_1 | 160 | 164 | PF16413 | 0.502 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.565 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.498 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 492 | 496 | PF00017 | 0.376 |
LIG_SH2_SRC | 234 | 237 | PF00017 | 0.472 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 471 | 475 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 519 | 523 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.473 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.460 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.511 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.523 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.526 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.494 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.624 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.518 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.484 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.697 |
LIG_SUMO_SIM_anti_2 | 363 | 370 | PF11976 | 0.470 |
LIG_SUMO_SIM_anti_2 | 453 | 460 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 334 | 339 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.522 |
LIG_TRAF2_1 | 476 | 479 | PF00917 | 0.516 |
LIG_TRFH_1 | 194 | 198 | PF08558 | 0.496 |
LIG_TYR_ITSM | 352 | 359 | PF00017 | 0.480 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.659 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.524 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.476 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.739 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.608 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.398 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.593 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.544 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.594 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.508 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.704 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.645 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.379 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.514 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.612 |
MOD_CK2_1 | 547 | 553 | PF00069 | 0.487 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.496 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.622 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.442 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.657 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.458 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.330 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.442 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.653 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.539 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.577 |
MOD_GlcNHglycan | 540 | 544 | PF01048 | 0.593 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.742 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.742 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.741 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.540 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.645 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.589 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.392 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.348 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.707 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.584 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.570 |
MOD_N-GLC_1 | 451 | 456 | PF02516 | 0.564 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.543 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.583 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.404 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.170 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.485 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.619 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.538 |
MOD_NEK2_2 | 547 | 552 | PF00069 | 0.485 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.510 |
MOD_PK_1 | 38 | 44 | PF00069 | 0.546 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.576 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.634 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.424 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.581 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.617 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.480 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.568 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.487 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.638 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.524 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.540 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.492 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.568 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.523 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.487 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.396 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.571 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.454 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.450 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.492 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.478 |
MOD_SUMO_rev_2 | 89 | 95 | PF00179 | 0.347 |
TRG_DiLeu_BaEn_1 | 364 | 369 | PF01217 | 0.396 |
TRG_DiLeu_BaLyEn_6 | 504 | 509 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 554 | 556 | PF00400 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 204 | 209 | PF00026 | 0.567 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHU3 | Leptomonas seymouri | 49% | 100% |
A0A1X0NJL9 | Trypanosomatidae | 29% | 100% |
A0A3R7NH89 | Trypanosoma rangeli | 30% | 100% |
A0A3S7WNM2 | Leishmania donovani | 90% | 99% |
A4H3F3 | Leishmania braziliensis | 72% | 100% |
A4HRQ7 | Leishmania infantum | 90% | 99% |
C9ZJ47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AJM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
V5BER3 | Trypanosoma cruzi | 28% | 100% |