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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0009295 | nucleoid | 2 | 1 |
GO:0042645 | mitochondrial nucleoid | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
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: A4I1Z0
Term | Name | Level | Count |
---|---|---|---|
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0070987 | error-free translesion synthesis | 8 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.340 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.340 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.315 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.337 |
CLV_Separin_Metazoa | 318 | 322 | PF03568 | 0.409 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.356 |
DEG_SCF_FBW7_1 | 128 | 133 | PF00400 | 0.568 |
DEG_SPOP_SBC_1 | 369 | 373 | PF00917 | 0.660 |
DOC_MAPK_gen_1 | 291 | 298 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 479 | 486 | PF00069 | 0.309 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.450 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.395 |
DOC_SPAK_OSR1_1 | 205 | 209 | PF12202 | 0.467 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.250 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.492 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 268 | 275 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 504 | 508 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.393 |
LIG_Actin_WH2_2 | 48 | 63 | PF00022 | 0.376 |
LIG_Actin_WH2_2 | 76 | 92 | PF00022 | 0.412 |
LIG_APCC_ABBA_1 | 484 | 489 | PF00400 | 0.387 |
LIG_BIR_III_2 | 125 | 129 | PF00653 | 0.546 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.593 |
LIG_BRCT_BRCA1_1 | 461 | 465 | PF00533 | 0.309 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.401 |
LIG_Clathr_ClatBox_1 | 432 | 436 | PF01394 | 0.309 |
LIG_CtBP_PxDLS_1 | 196 | 200 | PF00389 | 0.517 |
LIG_EVH1_2 | 202 | 206 | PF00568 | 0.478 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.610 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.333 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.511 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.387 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.460 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.567 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.422 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.372 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.362 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.370 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.355 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 77 | 86 | PF02991 | 0.394 |
LIG_LIR_LC3C_4 | 429 | 434 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.393 |
LIG_MYND_1 | 455 | 459 | PF01753 | 0.250 |
LIG_PTB_Apo_2 | 41 | 48 | PF02174 | 0.366 |
LIG_PTB_Phospho_1 | 41 | 47 | PF10480 | 0.364 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.326 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 408 | 411 | PF00017 | 0.309 |
LIG_SH2_SRC | 22 | 25 | PF00017 | 0.410 |
LIG_SH2_SRC | 408 | 411 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.288 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.522 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.608 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.455 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.337 |
LIG_SUMO_SIM_par_1 | 213 | 221 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 331 | 337 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 431 | 436 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.448 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.505 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.588 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.438 |
LIG_TRAF2_1 | 521 | 524 | PF00917 | 0.520 |
LIG_TYR_ITIM | 406 | 411 | PF00017 | 0.309 |
MOD_CDK_SPxK_1 | 371 | 377 | PF00069 | 0.567 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.582 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.750 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.307 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.508 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.547 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.669 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.250 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.503 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.584 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.376 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.615 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.309 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.523 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.545 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.738 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.285 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.580 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.558 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.561 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.520 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.505 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.702 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.250 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.250 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.393 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.590 |
MOD_GlcNHglycan | 531 | 535 | PF01048 | 0.690 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.781 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.525 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.365 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.338 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.517 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.609 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.632 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.385 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.454 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.436 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.468 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.571 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.277 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.518 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.454 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.558 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.309 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.548 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.553 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.564 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.484 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.512 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.598 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.250 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.414 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.544 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.605 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.352 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.341 |
MOD_PKB_1 | 528 | 536 | PF00069 | 0.560 |
MOD_Plk_2-3 | 273 | 279 | PF00069 | 0.619 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.425 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.462 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.362 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.620 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.647 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.567 |
MOD_SUMO_for_1 | 521 | 524 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 398 | 402 | PF00179 | 0.313 |
MOD_SUMO_rev_2 | 544 | 554 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_1 | 165 | 170 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.457 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.250 |
TRG_ENDOCYTIC_2 | 408 | 411 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.328 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.427 |
TRG_ER_diLys_1 | 573 | 578 | PF00400 | 0.655 |
TRG_NES_CRM1_1 | 27 | 41 | PF08389 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I464 | Leptomonas seymouri | 62% | 97% |
A0A1X0NSE4 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGW6 | Leishmania donovani | 100% | 100% |
A4HER3 | Leishmania braziliensis | 81% | 100% |
E9AY37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q9D6 | Leishmania major | 95% | 100% |