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 | yes | yes: 1, no: 6 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005829 | cytosol | 2 | 2 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HHH1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006289 | nucleotide-excision repair | 6 | 8 |
GO:0006508 | proteolysis | 4 | 8 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009056 | catabolic process | 2 | 8 |
GO:0009057 | macromolecule catabolic process | 4 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0010498 | proteasomal protein catabolic process | 5 | 8 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 8 |
GO:0030163 | protein catabolic process | 4 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044248 | cellular catabolic process | 3 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 8 |
GO:1901575 | organic substance catabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0003684 | damaged DNA binding | 5 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0005515 | protein binding | 2 | 2 |
GO:0031593 | polyubiquitin modification-dependent protein binding | 4 | 2 |
GO:0032182 | ubiquitin-like protein binding | 3 | 2 |
GO:0043130 | ubiquitin binding | 4 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0070628 | proteasome binding | 3 | 1 |
GO:0140030 | modification-dependent protein binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.676 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 135 | 137 | PF00082 | 0.722 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.478 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.410 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.531 |
DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.410 |
DOC_PP1_RVXF_1 | 375 | 381 | PF00149 | 0.312 |
DOC_PP4_FxxP_1 | 129 | 132 | PF00568 | 0.532 |
DOC_PP4_FxxP_1 | 395 | 398 | PF00568 | 0.510 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 90 | 97 | PF00244 | 0.413 |
LIG_BIR_III_4 | 330 | 334 | PF00653 | 0.524 |
LIG_EH1_1 | 2 | 10 | PF00400 | 0.455 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.362 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.446 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.413 |
LIG_Integrin_RGD_1 | 300 | 302 | PF01839 | 0.491 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 221 | 227 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 231 | 237 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.571 |
LIG_PAM2_1 | 47 | 59 | PF00658 | 0.347 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.480 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.552 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.794 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 101 | 107 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 196 | 201 | PF11976 | 0.506 |
LIG_SUMO_SIM_anti_2 | 231 | 238 | PF11976 | 0.512 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.670 |
LIG_TRAF2_1 | 164 | 167 | PF00917 | 0.658 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.420 |
LIG_TRAF2_1 | 355 | 358 | PF00917 | 0.477 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.529 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.541 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.694 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.664 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.592 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.749 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.612 |
MOD_GlcNHglycan | 159 | 165 | PF01048 | 0.599 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.538 |
MOD_GlcNHglycan | 315 | 319 | PF01048 | 0.579 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.698 |
MOD_GlcNHglycan | 66 | 71 | PF01048 | 0.741 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.544 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.682 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.451 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.551 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.693 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.597 |
MOD_N-GLC_1 | 108 | 113 | PF02516 | 0.630 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.485 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.748 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.480 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.626 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.538 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.461 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.600 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.373 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.479 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.636 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.488 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.564 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.517 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.550 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.609 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.754 |
MOD_Plk_2-3 | 263 | 269 | PF00069 | 0.653 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.493 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.532 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.517 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.522 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.506 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.519 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.627 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.706 |
MOD_SUMO_rev_2 | 356 | 363 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.560 |
TRG_DiLeu_BaEn_4 | 160 | 166 | PF01217 | 0.667 |
TRG_DiLeu_BaEn_4 | 262 | 268 | PF01217 | 0.629 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.422 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.722 |
TRG_NLS_MonoExtC_3 | 134 | 140 | PF00514 | 0.681 |
TRG_NLS_MonoExtN_4 | 132 | 139 | PF00514 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I958 | Leptomonas seymouri | 61% | 100% |
A0A3Q8IFF1 | Leishmania donovani | 77% | 100% |
A4I4M0 | Leishmania infantum | 77% | 100% |
E9AE18 | Leishmania major | 75% | 98% |
E9ALR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
V5B988 | Trypanosoma cruzi | 28% | 100% |