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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000785 | chromatin | 2 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 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: Q4QD07
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 10 |
GO:0007059 | chromosome segregation | 2 | 10 |
GO:0007062 | sister chromatid cohesion | 3 | 10 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 2 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0022402 | cell cycle process | 2 | 10 |
GO:0022414 | reproductive process | 1 | 10 |
GO:0045132 | meiotic chromosome segregation | 3 | 10 |
GO:0051276 | chromosome organization | 5 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0098813 | nuclear chromosome segregation | 3 | 10 |
GO:1903046 | meiotic cell cycle process | 2 | 10 |
GO:1903047 | mitotic cell cycle process | 3 | 10 |
GO:0000070 | mitotic sister chromatid segregation | 4 | 8 |
GO:0000819 | sister chromatid segregation | 4 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0008080 | N-acetyltransferase activity | 6 | 2 |
GO:0016407 | acetyltransferase activity | 5 | 10 |
GO:0016410 | N-acyltransferase activity | 5 | 2 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016746 | acyltransferase activity | 3 | 10 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 10 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 2 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.715 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.678 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.642 |
CLV_PCSK_PC7_1 | 70 | 76 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.480 |
DEG_SCF_FBW7_1 | 197 | 204 | PF00400 | 0.520 |
DEG_SCF_FBW7_1 | 211 | 217 | PF00400 | 0.407 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.505 |
DOC_MAPK_gen_1 | 256 | 265 | PF00069 | 0.424 |
DOC_PP1_RVXF_1 | 245 | 251 | PF00149 | 0.561 |
DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.526 |
DOC_PP4_FxxP_1 | 276 | 279 | PF00568 | 0.498 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.479 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.591 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 183 | 189 | PF00244 | 0.614 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.708 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.578 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.382 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.708 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.687 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.533 |
LIG_REV1ctd_RIR_1 | 64 | 74 | PF16727 | 0.546 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.580 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.602 |
LIG_SUMO_SIM_par_1 | 216 | 223 | PF11976 | 0.580 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.481 |
LIG_TYR_ITIM | 260 | 265 | PF00017 | 0.556 |
LIG_TYR_ITIM | 272 | 277 | PF00017 | 0.571 |
MOD_CDK_SPxxK_3 | 249 | 256 | PF00069 | 0.591 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.506 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.301 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.644 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.565 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.555 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.508 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.665 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.659 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.571 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.534 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.710 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.391 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.639 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.715 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.374 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.710 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.740 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.531 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.528 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.711 |
MOD_NEK2_2 | 110 | 115 | PF00069 | 0.469 |
MOD_OFUCOSY | 212 | 218 | PF10250 | 0.539 |
MOD_PKA_1 | 73 | 79 | PF00069 | 0.609 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.600 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.698 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.562 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.459 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.554 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.583 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.662 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.415 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.530 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.492 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.594 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.584 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.561 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.531 |
TRG_NLS_MonoExtC_3 | 72 | 77 | PF00514 | 0.676 |
TRG_NLS_MonoExtN_4 | 70 | 77 | PF00514 | 0.709 |
TRG_NLS_MonoExtN_4 | 98 | 105 | PF00514 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.590 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4N8 | Leptomonas seymouri | 38% | 100% |
A0A1X0NWH5 | Trypanosomatidae | 31% | 93% |
A0A3S7WVV5 | Leishmania donovani | 87% | 100% |
A0A422MWP0 | Trypanosoma rangeli | 34% | 100% |
A4HYS2 | Leishmania infantum | 87% | 100% |
E9AI91 | Leishmania braziliensis | 71% | 99% |
E9AUH7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5DS57 | Trypanosoma cruzi | 33% | 100% |