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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043228 | non-membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AN16
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.695 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.726 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.778 |
CLV_Separin_Metazoa | 216 | 220 | PF03568 | 0.430 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.829 |
DOC_MAPK_gen_1 | 113 | 121 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 203 | 211 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 113 | 121 | PF00069 | 0.504 |
DOC_PP1_RVXF_1 | 189 | 195 | PF00149 | 0.376 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.814 |
DOC_USP7_UBL2_3 | 114 | 118 | PF12436 | 0.737 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.385 |
DOC_USP7_UBL2_3 | 229 | 233 | PF12436 | 0.389 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.753 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.716 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.665 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.676 |
LIG_CtBP_PxDLS_1 | 240 | 246 | PF00389 | 0.424 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.768 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.692 |
LIG_MYND_1 | 84 | 88 | PF01753 | 0.513 |
LIG_SH2_STAT3 | 51 | 54 | PF00017 | 0.706 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.569 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.711 |
LIG_SxIP_EBH_1 | 80 | 93 | PF03271 | 0.807 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.584 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.536 |
LIG_WW_3 | 154 | 158 | PF00397 | 0.499 |
MOD_CDK_SPK_2 | 113 | 118 | PF00069 | 0.699 |
MOD_CDK_SPxxK_3 | 34 | 41 | PF00069 | 0.659 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.796 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.641 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.725 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.583 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.664 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.594 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.604 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.530 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.717 |
MOD_Cter_Amidation | 143 | 146 | PF01082 | 0.704 |
MOD_Cter_Amidation | 39 | 42 | PF01082 | 0.711 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.815 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.508 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.579 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.814 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.769 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.554 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.704 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.704 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.440 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.653 |
MOD_PKA_1 | 157 | 163 | PF00069 | 0.510 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.750 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.709 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.430 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.717 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.516 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.639 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.746 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.640 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.617 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.751 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.717 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 22 | 27 | PF00026 | 0.720 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4J8F0 | Bodo saltans | 42% | 100% |
A0A1X0NQ23 | Trypanosomatidae | 52% | 100% |
A0A3S5H6F2 | Leishmania donovani | 89% | 100% |
A4H5Z2 | Leishmania braziliensis | 75% | 98% |
A4HUB7 | Leishmania infantum | 89% | 100% |
Q4QHL0 | Leishmania major | 89% | 100% |