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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AXC2
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 1 |
GO:0002097 | tRNA wobble base modification | 7 | 1 |
GO:0002098 | tRNA wobble uridine modification | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0030488 | tRNA methylation | 5 | 1 |
GO:0032259 | methylation | 2 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043414 | macromolecule methylation | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.542 |
CLV_MEL_PAP_1 | 72 | 78 | PF00089 | 0.411 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.505 |
CLV_PCSK_FUR_1 | 303 | 307 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.336 |
CLV_Separin_Metazoa | 346 | 350 | PF03568 | 0.493 |
CLV_Separin_Metazoa | 439 | 443 | PF03568 | 0.346 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.467 |
DOC_CKS1_1 | 291 | 296 | PF01111 | 0.431 |
DOC_CKS1_1 | 368 | 373 | PF01111 | 0.397 |
DOC_CYCLIN_RxL_1 | 371 | 382 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 327 | 333 | PF00134 | 0.337 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 73 | 80 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 67 | 76 | PF00069 | 0.440 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.385 |
DOC_PP1_RVXF_1 | 458 | 465 | PF00149 | 0.357 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.303 |
DOC_PP2B_LxvP_1 | 387 | 390 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 431 | 434 | PF13499 | 0.518 |
DOC_PP2B_LxvP_1 | 6 | 9 | PF13499 | 0.417 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.422 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.498 |
DOC_PP4_FxxP_1 | 480 | 483 | PF00568 | 0.367 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.385 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.648 |
DOC_USP7_UBL2_3 | 274 | 278 | PF12436 | 0.456 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 442 | 446 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 73 | 79 | PF00244 | 0.408 |
LIG_APCC_ABBA_1 | 476 | 481 | PF00400 | 0.453 |
LIG_Clathr_ClatBox_1 | 288 | 292 | PF01394 | 0.442 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.446 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.630 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.455 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.453 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.443 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.479 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.491 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.552 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.470 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.400 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.426 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.535 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.344 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.368 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.433 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.379 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.511 |
LIG_Integrin_isoDGR_2 | 18 | 20 | PF01839 | 0.429 |
LIG_LIR_Apic_2 | 477 | 483 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 118 | 129 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 444 | 453 | PF02991 | 0.493 |
LIG_LIR_LC3C_4 | 323 | 326 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.282 |
LIG_Pex14_2 | 513 | 517 | PF04695 | 0.413 |
LIG_REV1ctd_RIR_1 | 477 | 482 | PF16727 | 0.349 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.397 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.535 |
LIG_SH2_CRK | 415 | 419 | PF00017 | 0.360 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.420 |
LIG_SH2_NCK_1 | 415 | 419 | PF00017 | 0.360 |
LIG_SH2_SRC | 121 | 124 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.391 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.497 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.388 |
LIG_SUMO_SIM_anti_2 | 285 | 293 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 323 | 328 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 170 | 177 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 285 | 293 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 403 | 410 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 85 | 90 | PF11976 | 0.397 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.421 |
LIG_WRC_WIRS_1 | 486 | 491 | PF05994 | 0.357 |
MOD_CDK_SPK_2 | 367 | 372 | PF00069 | 0.373 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.400 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.392 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.494 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.488 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.566 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.372 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.419 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.390 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.473 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.467 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.460 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.547 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.367 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.644 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.269 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.477 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.404 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.400 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.414 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.547 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.456 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.345 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.409 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.493 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.376 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.379 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.398 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.399 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.545 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.472 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.665 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.452 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.422 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.498 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.420 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.395 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.431 |
MOD_NEK2_2 | 485 | 490 | PF00069 | 0.344 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.431 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.431 |
MOD_PK_1 | 170 | 176 | PF00069 | 0.485 |
MOD_PKA_1 | 466 | 472 | PF00069 | 0.393 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.384 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.580 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.500 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.374 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.527 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.382 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.485 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.448 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.480 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.473 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.377 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.448 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.412 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.431 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.413 |
MOD_SUMO_rev_2 | 337 | 343 | PF00179 | 0.370 |
TRG_DiLeu_BaEn_2 | 510 | 516 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 457 | 460 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 72 | 75 | PF00400 | 0.443 |
TRG_NES_CRM1_1 | 355 | 366 | PF08389 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 506 | 511 | PF00026 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PER9 | Leptomonas seymouri | 82% | 100% |
A0A0S4IU66 | Bodo saltans | 50% | 100% |
A0A1X0P4I4 | Trypanosomatidae | 64% | 100% |
A0A3R7NZ49 | Trypanosoma rangeli | 66% | 100% |
A0A3S5H7E2 | Leishmania donovani | 98% | 100% |
A4HDY7 | Leishmania braziliensis | 91% | 100% |
A4I188 | Leishmania infantum | 97% | 100% |
D0A5H3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 63% | 100% |
Q4QA50 | Leishmania major | 92% | 100% |
V5B7N0 | Trypanosoma cruzi | 65% | 100% |