Uncharacterized Protein, Uncharacterized
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4I420
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 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:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 326 | 330 | PF00656 | 0.605 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.442 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 297 | 299 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.655 |
CLV_PCSK_PC7_1 | 119 | 125 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.553 |
CLV_Separin_Metazoa | 222 | 226 | PF03568 | 0.486 |
DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.493 |
DOC_ANK_TNKS_1 | 224 | 231 | PF00023 | 0.475 |
DOC_CDC14_PxL_1 | 174 | 182 | PF14671 | 0.472 |
DOC_CDC14_PxL_1 | 408 | 416 | PF14671 | 0.477 |
DOC_CYCLIN_RxL_1 | 133 | 145 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 90 | 101 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 165 | 171 | PF00134 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.427 |
DOC_CYCLIN_yCln2_LP_2 | 287 | 293 | PF00134 | 0.419 |
DOC_CYCLIN_yCln2_LP_2 | 338 | 344 | PF00134 | 0.621 |
DOC_MAPK_gen_1 | 123 | 129 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 281 | 291 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 281 | 289 | PF00069 | 0.495 |
DOC_PP1_RVXF_1 | 184 | 191 | PF00149 | 0.369 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.427 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.451 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.528 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.718 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.656 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.572 |
LIG_Actin_WH2_2 | 282 | 299 | PF00022 | 0.470 |
LIG_APCC_ABBA_1 | 140 | 145 | PF00400 | 0.443 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.550 |
LIG_BIR_III_4 | 329 | 333 | PF00653 | 0.601 |
LIG_BRCT_BRCA1_1 | 81 | 85 | PF00533 | 0.510 |
LIG_CSL_BTD_1 | 287 | 290 | PF09270 | 0.461 |
LIG_DLG_GKlike_1 | 23 | 30 | PF00625 | 0.477 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.538 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.707 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.613 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.449 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.410 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.637 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.717 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.439 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.680 |
LIG_LIR_Apic_2 | 245 | 250 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 22 | 30 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 271 | 279 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.512 |
LIG_LIR_LC3C_4 | 239 | 243 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.361 |
LIG_LYPXL_S_1 | 381 | 385 | PF13949 | 0.476 |
LIG_LYPXL_yS_3 | 382 | 385 | PF13949 | 0.494 |
LIG_NRBOX | 198 | 204 | PF00104 | 0.475 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.460 |
LIG_SH3_1 | 246 | 252 | PF00018 | 0.492 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.446 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.528 |
LIG_SH3_CIN85_PxpxPR_1 | 52 | 57 | PF14604 | 0.578 |
LIG_SUMO_SIM_anti_2 | 103 | 108 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 138 | 145 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 389 | 395 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 4 | 10 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.580 |
LIG_TYR_ITIM | 306 | 311 | PF00017 | 0.393 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.411 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.509 |
MOD_CDK_SPK_2 | 52 | 57 | PF00069 | 0.578 |
MOD_CDK_SPxxK_3 | 351 | 358 | PF00069 | 0.628 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.469 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.523 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.734 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.619 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.628 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.544 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.714 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.417 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.601 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.692 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.564 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.665 |
MOD_Cter_Amidation | 14 | 17 | PF01082 | 0.575 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.584 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.481 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.568 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.698 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.573 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.713 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.598 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.599 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.524 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.513 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.579 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.509 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.507 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.699 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.516 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.637 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.620 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.571 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.461 |
MOD_N-GLC_2 | 418 | 420 | PF02516 | 0.530 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.425 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.461 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.559 |
MOD_OFUCOSY | 320 | 325 | PF10250 | 0.512 |
MOD_PIKK_1 | 172 | 178 | PF00454 | 0.502 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.566 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.609 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.571 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.609 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.659 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.564 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.460 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.523 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.460 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.651 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.577 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.665 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.650 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.666 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.636 |
MOD_SUMO_for_1 | 150 | 153 | PF00179 | 0.608 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 232 | 234 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.435 |
TRG_NES_CRM1_1 | 409 | 421 | PF08389 | 0.443 |
TRG_NLS_MonoCore_2 | 432 | 437 | PF00514 | 0.623 |
TRG_NLS_MonoExtC_3 | 433 | 438 | PF00514 | 0.625 |
TRG_NLS_MonoExtN_4 | 433 | 438 | PF00514 | 0.746 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4Z3 | Leptomonas seymouri | 45% | 93% |
A0A0S4IUX7 | Bodo saltans | 25% | 98% |
A0A1X0NQH2 | Trypanosomatidae | 28% | 100% |
A0A3S7X213 | Leishmania donovani | 100% | 100% |
A0A422N0P3 | Trypanosoma rangeli | 28% | 99% |
A4HGY8 | Leishmania braziliensis | 77% | 100% |
D0A8Y9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 98% |
E9B0A7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q7X7 | Leishmania major | 94% | 100% |
V5ATM8 | Trypanosoma cruzi | 29% | 100% |