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:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
Related structures:
AlphaFold database: A4HNZ2
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.758 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.670 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.471 |
DOC_CYCLIN_yCln2_LP_2 | 216 | 222 | PF00134 | 0.233 |
DOC_MAPK_gen_1 | 176 | 182 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 51 | 60 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 25 | 34 | PF00069 | 0.483 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.793 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.508 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.754 |
DOC_USP7_UBL2_3 | 259 | 263 | PF12436 | 0.704 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.512 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.606 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.499 |
LIG_14-3-3_CterR_2 | 264 | 267 | PF00244 | 0.559 |
LIG_deltaCOP1_diTrp_1 | 74 | 78 | PF00928 | 0.561 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.576 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.554 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.513 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.473 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.673 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.583 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.531 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.531 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.695 |
LIG_LIR_Nem_3 | 230 | 235 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.486 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.561 |
LIG_SH3_2 | 178 | 183 | PF14604 | 0.781 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.756 |
LIG_SH3_4 | 259 | 266 | PF00018 | 0.707 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.591 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.608 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.699 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.531 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.723 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.531 |
MOD_Cter_Amidation | 49 | 52 | PF01082 | 0.361 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.802 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.560 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.691 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.276 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.632 |
MOD_LATS_1 | 231 | 237 | PF00433 | 0.591 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.540 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.770 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.391 |
MOD_OFUCOSY | 44 | 49 | PF10250 | 0.331 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.515 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.555 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.555 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.421 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.607 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.456 |
TRG_ER_diLys_1 | 263 | 267 | PF00400 | 0.553 |
TRG_NLS_MonoCore_2 | 262 | 267 | PF00514 | 0.715 |
TRG_NLS_MonoExtN_4 | 260 | 267 | PF00514 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA52 | Leptomonas seymouri | 61% | 100% |
A0A0S4J2P2 | Bodo saltans | 39% | 97% |
A0A1X0P7R0 | Trypanosomatidae | 42% | 100% |
A0A3S5H819 | Leishmania donovani | 74% | 93% |
A4ICK1 | Leishmania infantum | 74% | 93% |
D0A369 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ASQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q1U1 | Leishmania major | 76% | 100% |