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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q8J9
Term | Name | Level | Count |
---|---|---|---|
GO:0000725 | recombinational repair | 6 | 7 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006310 | DNA recombination | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.304 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.242 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.437 |
DOC_CYCLIN_RxL_1 | 138 | 150 | PF00134 | 0.513 |
DOC_PP2B_LxvP_1 | 113 | 116 | PF13499 | 0.304 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.304 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.312 |
LIG_APCC_ABBA_1 | 84 | 89 | PF00400 | 0.245 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.582 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.319 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.327 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.391 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.256 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.633 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.420 |
LIG_Integrin_RGD_1 | 173 | 175 | PF01839 | 0.507 |
LIG_IRF3_LxIS_1 | 90 | 96 | PF10401 | 0.325 |
LIG_LIR_Apic_2 | 189 | 194 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 62 | 71 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.378 |
LIG_LYPXL_yS_3 | 75 | 78 | PF13949 | 0.304 |
LIG_MYND_2 | 100 | 104 | PF01753 | 0.369 |
LIG_NRBOX | 109 | 115 | PF00104 | 0.304 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.304 |
LIG_SUMO_SIM_anti_2 | 242 | 248 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 88 | 94 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 51 | 58 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 88 | 97 | PF11976 | 0.304 |
LIG_WRC_WIRS_1 | 178 | 183 | PF05994 | 0.597 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.660 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.391 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.563 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.426 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.592 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.616 |
MOD_GlcNHglycan | 155 | 159 | PF01048 | 0.584 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.608 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.647 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.392 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.304 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.304 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.622 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.623 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.544 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.316 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.432 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.600 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.589 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.243 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.595 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.321 |
MOD_NEK2_2 | 177 | 182 | PF00069 | 0.508 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.304 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.599 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.315 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.502 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.294 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.304 |
MOD_Plk_2-3 | 2 | 8 | PF00069 | 0.426 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.738 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.426 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.304 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 206 | 211 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1R0 | Leptomonas seymouri | 49% | 97% |
A0A3S7X1B4 | Leishmania donovani | 94% | 100% |
A4HGB1 | Leishmania braziliensis | 72% | 100% |
A4I3E5 | Leishmania infantum | 94% | 100% |
E9AZN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |