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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACD9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.560 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.498 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.690 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.550 |
DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.785 |
DOC_CYCLIN_RxL_1 | 197 | 207 | PF00134 | 0.580 |
DOC_MAPK_DCC_7 | 171 | 181 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 197 | 205 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 80 | 90 | PF00069 | 0.719 |
DOC_MAPK_MEF2A_6 | 172 | 181 | PF00069 | 0.563 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.754 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 136 | 140 | PF00244 | 0.807 |
LIG_14-3-3_CanoR_1 | 182 | 189 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.636 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.775 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.570 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.597 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.823 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.574 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.584 |
LIG_NRBOX | 51 | 57 | PF00104 | 0.517 |
LIG_PCNA_yPIPBox_3 | 80 | 88 | PF02747 | 0.632 |
LIG_PDZ_Class_3 | 310 | 315 | PF00595 | 0.589 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.443 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.770 |
LIG_SUMO_SIM_anti_2 | 86 | 91 | PF11976 | 0.618 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.631 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.591 |
LIG_WRPW_2 | 105 | 108 | PF00400 | 0.646 |
MOD_CDK_SPxxK_3 | 190 | 197 | PF00069 | 0.631 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.773 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.769 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.796 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.825 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.821 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.550 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.675 |
MOD_CMANNOS | 108 | 111 | PF00535 | 0.643 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.549 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.721 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.640 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.732 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.529 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.679 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.775 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.711 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.591 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.759 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.726 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.647 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.739 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.642 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.725 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.657 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.642 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.596 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.596 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.635 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.605 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.598 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.578 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.605 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.696 |
MOD_SUMO_for_1 | 231 | 234 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 161 | 168 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 41 | 49 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 63 | 68 | PF00179 | 0.654 |
TRG_DiLeu_BaEn_1 | 199 | 204 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_4 | 187 | 193 | PF01217 | 0.635 |
TRG_DiLeu_BaEn_4 | 44 | 50 | PF01217 | 0.585 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.595 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.470 |
TRG_NLS_MonoCore_2 | 170 | 175 | PF00514 | 0.665 |
TRG_NLS_MonoExtN_4 | 169 | 176 | PF00514 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.697 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 229 | 234 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W5 | Leptomonas seymouri | 52% | 100% |
A0A0S4JF25 | Bodo saltans | 24% | 100% |
A0A1X0NJL7 | Trypanosomatidae | 38% | 95% |
A0A3S5H512 | Leishmania donovani | 91% | 100% |
A0A422NAY0 | Trypanosoma rangeli | 33% | 95% |
A4H3F6 | Leishmania braziliensis | 75% | 100% |
A4HRR0 | Leishmania infantum | 91% | 100% |
C9ZJ49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AJM7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5D620 | Trypanosoma cruzi | 35% | 98% |