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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJM7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.760 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.549 |
DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.773 |
DOC_CKS1_1 | 11 | 16 | PF01111 | 0.763 |
DOC_MAPK_DCC_7 | 170 | 180 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 80 | 90 | PF00069 | 0.700 |
DOC_MAPK_MEF2A_6 | 171 | 180 | PF00069 | 0.577 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.766 |
LIG_14-3-3_CanoR_1 | 181 | 188 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 48 | 56 | PF00244 | 0.628 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.501 |
LIG_CtBP_PxDLS_1 | 177 | 181 | PF00389 | 0.497 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.759 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.569 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.808 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.562 |
LIG_LIR_Nem_3 | 218 | 224 | PF02991 | 0.579 |
LIG_NRBOX | 51 | 57 | PF00104 | 0.500 |
LIG_PCNA_yPIPBox_3 | 80 | 88 | PF02747 | 0.615 |
LIG_PDZ_Class_3 | 309 | 314 | PF00595 | 0.582 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.465 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.537 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.746 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.722 |
LIG_SUMO_SIM_anti_2 | 86 | 91 | PF11976 | 0.595 |
LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.638 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.555 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.576 |
LIG_UBA3_1 | 67 | 71 | PF00899 | 0.363 |
LIG_WRPW_2 | 105 | 108 | PF00400 | 0.626 |
LIG_WW_2 | 14 | 17 | PF00397 | 0.606 |
MOD_CDK_SPxxK_3 | 115 | 122 | PF00069 | 0.560 |
MOD_CDK_SPxxK_3 | 189 | 196 | PF00069 | 0.631 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.723 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.753 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.809 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.812 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.542 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.672 |
MOD_CMANNOS | 108 | 111 | PF00535 | 0.636 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.548 |
MOD_GlcNHglycan | 127 | 132 | PF01048 | 0.648 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.556 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.634 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.733 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.525 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.633 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.715 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.519 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.672 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.673 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.722 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.728 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.746 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.715 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.644 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.616 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.736 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.640 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.714 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.640 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.594 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.595 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.587 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.600 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.690 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 160 | 167 | PF00179 | 0.595 |
MOD_SUMO_rev_2 | 245 | 252 | PF00179 | 0.338 |
MOD_SUMO_rev_2 | 41 | 49 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 63 | 68 | PF00179 | 0.637 |
TRG_DiLeu_BaEn_1 | 198 | 203 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_4 | 186 | 192 | PF01217 | 0.634 |
TRG_DiLeu_BaEn_4 | 44 | 50 | PF01217 | 0.582 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.592 |
TRG_NLS_MonoCore_2 | 169 | 174 | PF00514 | 0.682 |
TRG_NLS_MonoExtN_4 | 168 | 175 | PF00514 | 0.608 |
TRG_Pf-PMV_PEXEL_1 | 123 | 127 | PF00026 | 0.694 |
TRG_Pf-PMV_PEXEL_1 | 181 | 185 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 228 | 233 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3W5 | Leptomonas seymouri | 50% | 100% |
A0A0S4JF25 | Bodo saltans | 26% | 100% |
A0A1X0NJL7 | Trypanosomatidae | 38% | 95% |
A0A3S5H512 | Leishmania donovani | 90% | 100% |
A0A422NAY0 | Trypanosoma rangeli | 34% | 95% |
A4H3F6 | Leishmania braziliensis | 77% | 96% |
A4HRR0 | Leishmania infantum | 90% | 100% |
C9ZJ49 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9ACD9 | Leishmania major | 90% | 100% |
V5D620 | Trypanosoma cruzi | 39% | 98% |