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 |
Related structures:
AlphaFold database: E9AXA6
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 | 10 |
GO:0016874 | ligase activity | 2 | 10 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 10 |
GO:0016880 | acid-ammonia (or amide) ligase activity | 4 | 10 |
GO:0017178 | diphthine-ammonia ligase activity | 5 | 10 |
GO:0000166 | nucleotide binding | 3 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0036094 | small molecule binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.267 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.342 |
CLV_PCSK_PC7_1 | 82 | 88 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.310 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.270 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.318 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.292 |
DOC_CYCLIN_RxL_1 | 533 | 544 | PF00134 | 0.406 |
DOC_CYCLIN_yCln2_LP_2 | 225 | 231 | PF00134 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 320 | 326 | PF00134 | 0.413 |
DOC_MAPK_gen_1 | 279 | 287 | PF00069 | 0.431 |
DOC_PP1_RVXF_1 | 138 | 144 | PF00149 | 0.303 |
DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.437 |
DOC_PP2B_LxvP_1 | 432 | 435 | PF13499 | 0.333 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.363 |
DOC_PP4_FxxP_1 | 385 | 388 | PF00568 | 0.370 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.333 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 474 | 484 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 536 | 541 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 550 | 554 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 599 | 603 | PF00244 | 0.388 |
LIG_Actin_WH2_2 | 65 | 83 | PF00022 | 0.270 |
LIG_BIR_III_2 | 290 | 294 | PF00653 | 0.276 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.582 |
LIG_BRCT_BRCA1_1 | 472 | 476 | PF00533 | 0.308 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.300 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.242 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.246 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.344 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.327 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.286 |
LIG_FHA_1 | 573 | 579 | PF00498 | 0.324 |
LIG_FHA_1 | 593 | 599 | PF00498 | 0.408 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.363 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.363 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.245 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.382 |
LIG_LIR_Apic_2 | 347 | 351 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 152 | 161 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 535 | 545 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 58 | 69 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 535 | 540 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 544 | 548 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.246 |
LIG_PDZ_Class_3 | 610 | 615 | PF00595 | 0.477 |
LIG_Pex14_2 | 381 | 385 | PF04695 | 0.350 |
LIG_Pex14_2 | 472 | 476 | PF04695 | 0.210 |
LIG_Pex14_2 | 541 | 545 | PF04695 | 0.487 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.270 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.406 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.246 |
LIG_SH2_STAT3 | 97 | 100 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.358 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.360 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.301 |
LIG_SUMO_SIM_anti_2 | 238 | 244 | PF11976 | 0.328 |
LIG_SUMO_SIM_anti_2 | 3 | 8 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.401 |
LIG_TRAF2_1 | 101 | 104 | PF00917 | 0.311 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.306 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.208 |
LIG_TRAF2_1 | 610 | 613 | PF00917 | 0.578 |
LIG_TRFH_1 | 301 | 305 | PF08558 | 0.365 |
MOD_CDK_SPxK_1 | 477 | 483 | PF00069 | 0.363 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.267 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.634 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.501 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.348 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.245 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.372 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.362 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.444 |
MOD_DYRK1A_RPxSP_1 | 376 | 380 | PF00069 | 0.343 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.306 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.343 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.612 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.677 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.719 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.403 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.461 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.447 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.246 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.427 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.308 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.402 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.291 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.363 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.213 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.594 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.683 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.428 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.312 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.497 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.566 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.273 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.383 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.386 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.248 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.232 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.266 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.288 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.487 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.455 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.542 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.438 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.420 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.469 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.363 |
MOD_NEK2_2 | 392 | 397 | PF00069 | 0.292 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.502 |
MOD_PIKK_1 | 507 | 513 | PF00454 | 0.477 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.376 |
MOD_PK_1 | 179 | 185 | PF00069 | 0.270 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.363 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.550 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.512 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.378 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.508 |
MOD_Plk_1 | 220 | 226 | PF00069 | 0.335 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.396 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.349 |
MOD_Plk_1 | 91 | 97 | PF00069 | 0.363 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.308 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.230 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.306 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.249 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.418 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.308 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.342 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.363 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.371 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.362 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.426 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.336 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.416 |
TRG_DiLeu_BaEn_1 | 272 | 277 | PF01217 | 0.236 |
TRG_DiLeu_BaEn_4 | 272 | 278 | PF01217 | 0.239 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.147 |
TRG_DiLeu_BaLyEn_6 | 290 | 295 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.270 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.213 |
TRG_ER_diArg_1 | 464 | 466 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.246 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.246 |
TRG_NES_CRM1_1 | 162 | 174 | PF08389 | 0.327 |
TRG_NES_CRM1_1 | 596 | 609 | PF08389 | 0.368 |
TRG_Pf-PMV_PEXEL_1 | 193 | 197 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 87 | 92 | PF00026 | 0.267 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEV4 | Leptomonas seymouri | 59% | 100% |
A0A1X0P4I2 | Trypanosomatidae | 39% | 100% |
A0A3R7K7F7 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WYW4 | Leishmania donovani | 89% | 100% |
A4HDX7 | Leishmania braziliensis | 79% | 100% |
A4I172 | Leishmania infantum | 89% | 100% |
D0A5F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4QA66 | Leishmania major | 89% | 100% |
Q9USQ7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |