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) | yes | yes: 3 |
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: 1, no: 6 |
NetGPI | no | yes: 0, no: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I710
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0000774 | adenyl-nucleotide exchange factor activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0060590 | ATPase regulator activity | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 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 | 172 | 176 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.316 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.488 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 91 | 93 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.373 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.485 |
DOC_ANK_TNKS_1 | 439 | 446 | PF00023 | 0.432 |
DOC_CYCLIN_RxL_1 | 91 | 101 | PF00134 | 0.362 |
DOC_CYCLIN_yCln2_LP_2 | 213 | 219 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 91 | 98 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 363 | 370 | PF00149 | 0.329 |
DOC_PP1_RVXF_1 | 449 | 455 | PF00149 | 0.378 |
DOC_PP1_RVXF_1 | 92 | 99 | PF00149 | 0.407 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.438 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 312 | 318 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 360 | 369 | PF00244 | 0.286 |
LIG_14-3-3_CterR_2 | 460 | 462 | PF00244 | 0.404 |
LIG_APCC_ABBA_1 | 197 | 202 | PF00400 | 0.338 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.506 |
LIG_Clathr_ClatBox_1 | 97 | 101 | PF01394 | 0.409 |
LIG_deltaCOP1_diTrp_1 | 129 | 137 | PF00928 | 0.393 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.380 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.390 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.421 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.443 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.381 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.405 |
LIG_Integrin_RGD_1 | 179 | 181 | PF01839 | 0.585 |
LIG_LIR_Gen_1 | 136 | 143 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 201 | 206 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.452 |
LIG_NRBOX | 272 | 278 | PF00104 | 0.346 |
LIG_Pex14_1 | 133 | 137 | PF04695 | 0.341 |
LIG_PTAP_UEV_1 | 30 | 35 | PF05743 | 0.621 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.352 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.649 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.442 |
LIG_SUMO_SIM_anti_2 | 301 | 309 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 331 | 336 | PF11976 | 0.440 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.328 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.519 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.504 |
MOD_CDC14_SPxK_1 | 88 | 91 | PF00782 | 0.437 |
MOD_CDK_SPK_2 | 412 | 417 | PF00069 | 0.392 |
MOD_CDK_SPxK_1 | 85 | 91 | PF00069 | 0.452 |
MOD_CDK_SPxxK_3 | 85 | 92 | PF00069 | 0.444 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.527 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.342 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.468 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.593 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.580 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.452 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.513 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.592 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.478 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.589 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.412 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.262 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.433 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.452 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.629 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.454 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.514 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.571 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.439 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.612 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.480 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.292 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.511 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.464 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.332 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.613 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.478 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.490 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.688 |
MOD_N-GLC_2 | 13 | 15 | PF02516 | 0.419 |
MOD_N-GLC_2 | 28 | 30 | PF02516 | 0.594 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.555 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.508 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.357 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.381 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.251 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.419 |
MOD_PKA_1 | 360 | 366 | PF00069 | 0.246 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.326 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.493 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.554 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.423 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.363 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.390 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.390 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.390 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.496 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.437 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.452 |
MOD_SUMO_rev_2 | 101 | 109 | PF00179 | 0.470 |
TRG_DiLeu_BaEn_3 | 122 | 128 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 381 | 387 | PF01217 | 0.343 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.334 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 351 | 356 | PF01217 | 0.439 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.451 |
TRG_NES_CRM1_1 | 236 | 250 | PF08389 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXH6 | Leptomonas seymouri | 47% | 100% |
A0A3S7X4Q0 | Leishmania donovani | 99% | 100% |
A4HJL0 | Leishmania braziliensis | 65% | 100% |
E9B228 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q634 | Leishmania major | 87% | 100% |
V5BA98 | Trypanosoma cruzi | 27% | 100% |