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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000785 | chromatin | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 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 |
Related structures:
AlphaFold database: E9AUH7
Term | Name | Level | Count |
---|---|---|---|
GO:0000070 | mitotic sister chromatid segregation | 4 | 10 |
GO:0000819 | sister chromatid segregation | 4 | 10 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0007059 | chromosome segregation | 2 | 11 |
GO:0007062 | sister chromatid cohesion | 3 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0022402 | cell cycle process | 2 | 11 |
GO:0022414 | reproductive process | 1 | 11 |
GO:0045132 | meiotic chromosome segregation | 3 | 11 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0098813 | nuclear chromosome segregation | 3 | 11 |
GO:1903046 | meiotic cell cycle process | 2 | 11 |
GO:1903047 | mitotic cell cycle process | 3 | 11 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016407 | acetyltransferase activity | 5 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016746 | acyltransferase activity | 3 | 11 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 11 |
GO:0008080 | N-acetyltransferase activity | 6 | 1 |
GO:0016410 | N-acyltransferase activity | 5 | 1 |
GO:0034212 | peptide N-acetyltransferase activity | 7 | 1 |
GO:0061733 | peptide-lysine-N-acetyltransferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 203 | 207 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.652 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.179 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.694 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.173 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.650 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.610 |
CLV_PCSK_PC7_1 | 70 | 76 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.478 |
DEG_SPOP_SBC_1 | 196 | 200 | PF00917 | 0.475 |
DOC_PP1_RVXF_1 | 245 | 251 | PF00149 | 0.548 |
DOC_PP4_FxxP_1 | 276 | 279 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.346 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.531 |
LIG_Actin_WH2_2 | 138 | 155 | PF00022 | 0.314 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.430 |
LIG_FHA_2 | 201 | 207 | PF00498 | 0.718 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.605 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.470 |
LIG_MYND_3 | 1 | 5 | PF01753 | 0.467 |
LIG_REV1ctd_RIR_1 | 64 | 74 | PF16727 | 0.510 |
LIG_SH2_CRK | 274 | 278 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 262 | 266 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.512 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 138 | 144 | PF11976 | 0.264 |
LIG_TYR_ITIM | 260 | 265 | PF00017 | 0.542 |
LIG_TYR_ITIM | 272 | 277 | PF00017 | 0.559 |
MOD_CDK_SPxxK_3 | 249 | 256 | PF00069 | 0.543 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.492 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.302 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.665 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.664 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.541 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.490 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.661 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.486 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.484 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.424 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.621 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.363 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.631 |
MOD_GlcNHglycan | 89 | 93 | PF01048 | 0.696 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.682 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.353 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.603 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.670 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.738 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.514 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.505 |
MOD_NEK2_2 | 109 | 114 | PF00069 | 0.446 |
MOD_OFUCOSY | 211 | 218 | PF10250 | 0.517 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.606 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.520 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.514 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.430 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.620 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.660 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.603 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.477 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.461 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.573 |
TRG_DiLeu_BaEn_4 | 5 | 11 | PF01217 | 0.440 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 262 | 265 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.547 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.514 |
TRG_NLS_MonoExtC_3 | 72 | 77 | PF00514 | 0.647 |
TRG_NLS_MonoExtN_4 | 70 | 77 | PF00514 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4N8 | Leptomonas seymouri | 35% | 100% |
A0A1X0NWH5 | Trypanosomatidae | 33% | 93% |
A0A3S7WVV5 | Leishmania donovani | 82% | 100% |
A0A422MWP0 | Trypanosoma rangeli | 35% | 100% |
A4HYS2 | Leishmania infantum | 82% | 100% |
C9ZIA6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AI91 | Leishmania braziliensis | 68% | 100% |
Q4QD07 | Leishmania major | 85% | 100% |
V5DS57 | Trypanosoma cruzi | 33% | 100% |