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 | 2 |
GO:0009295 | nucleoid | 2 | 2 |
GO:0042645 | mitochondrial nucleoid | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q9D6
Term | Name | Level | Count |
---|---|---|---|
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006301 | postreplication repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019985 | translesion synthesis | 7 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0070987 | error-free translesion synthesis | 8 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071897 | DNA biosynthetic process | 5 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.363 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.388 |
CLV_Separin_Metazoa | 319 | 323 | PF03568 | 0.466 |
DEG_SCF_FBW7_1 | 128 | 133 | PF00400 | 0.601 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.736 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 480 | 487 | PF00069 | 0.354 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.534 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.440 |
DOC_SPAK_OSR1_1 | 205 | 209 | PF12202 | 0.548 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.569 |
LIG_14-3-3_CanoR_1 | 152 | 162 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 505 | 509 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 75 | 83 | PF00244 | 0.441 |
LIG_Actin_WH2_2 | 48 | 63 | PF00022 | 0.427 |
LIG_Actin_WH2_2 | 76 | 92 | PF00022 | 0.464 |
LIG_APCC_ABBA_1 | 485 | 490 | PF00400 | 0.441 |
LIG_BIR_III_2 | 125 | 129 | PF00653 | 0.580 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.634 |
LIG_BRCT_BRCA1_1 | 462 | 466 | PF00533 | 0.354 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.448 |
LIG_Clathr_ClatBox_1 | 433 | 437 | PF01394 | 0.354 |
LIG_CtBP_PxDLS_1 | 196 | 200 | PF00389 | 0.580 |
LIG_EVH1_2 | 202 | 206 | PF00568 | 0.559 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.691 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.385 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.590 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.404 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.396 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.576 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.449 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.462 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.421 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 77 | 86 | PF02991 | 0.441 |
LIG_LIR_LC3C_4 | 430 | 435 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.441 |
LIG_MYND_1 | 456 | 460 | PF01753 | 0.295 |
LIG_PTB_Apo_2 | 41 | 48 | PF02174 | 0.419 |
LIG_PTB_Phospho_1 | 41 | 47 | PF10480 | 0.417 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.380 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.477 |
LIG_SH2_PTP2 | 409 | 412 | PF00017 | 0.354 |
LIG_SH2_SRC | 22 | 25 | PF00017 | 0.477 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.291 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.646 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.567 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.416 |
LIG_SUMO_SIM_par_1 | 213 | 221 | PF11976 | 0.590 |
LIG_SUMO_SIM_par_1 | 228 | 235 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 332 | 338 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 432 | 437 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 506 | 512 | PF11976 | 0.504 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.641 |
LIG_TRAF2_1 | 313 | 316 | PF00917 | 0.491 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.579 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.354 |
MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.576 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.594 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.623 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.757 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.402 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.617 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.565 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.656 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.296 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.551 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.631 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.424 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.721 |
MOD_CK2_1 | 470 | 476 | PF00069 | 0.354 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.641 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.623 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.774 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.347 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.694 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.667 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.684 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.656 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.636 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.691 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.302 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.313 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.445 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.682 |
MOD_GlcNHglycan | 532 | 536 | PF01048 | 0.759 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.822 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.578 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.410 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.387 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.595 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.640 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.697 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.423 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.481 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.482 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.594 |
MOD_N-GLC_1 | 288 | 293 | PF02516 | 0.614 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.337 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.576 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.498 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.573 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.354 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.608 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.628 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.608 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.595 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.595 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.650 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.295 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.453 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.647 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.399 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.388 |
MOD_PKB_1 | 529 | 537 | PF00069 | 0.622 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.663 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.536 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.530 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.458 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.704 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.729 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.576 |
MOD_SUMO_for_1 | 522 | 525 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 399 | 403 | PF00179 | 0.358 |
MOD_SUMO_rev_2 | 545 | 555 | PF00179 | 0.631 |
TRG_DiLeu_BaEn_1 | 165 | 170 | PF01217 | 0.597 |
TRG_DiLeu_BaEn_1 | 211 | 216 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 316 | 321 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 453 | 458 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 101 | 103 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.386 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 83 | 85 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.563 |
TRG_ER_diLys_1 | 574 | 579 | PF00400 | 0.695 |
TRG_NES_CRM1_1 | 27 | 41 | PF08389 | 0.374 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I464 | Leptomonas seymouri | 61% | 97% |
A0A1X0NSE4 | Trypanosomatidae | 32% | 100% |
A0A3Q8IGW6 | Leishmania donovani | 95% | 100% |
A4HER3 | Leishmania braziliensis | 79% | 97% |
A4I1Z0 | Leishmania infantum | 95% | 100% |
E9AY37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |