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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0016020 | membrane | 2 | 9 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031410 | cytoplasmic vesicle | 6 | 5 |
GO:0031982 | vesicle | 4 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0097708 | intracellular vesicle | 5 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9AFP6
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 5 |
GO:0016043 | cellular component organization | 3 | 5 |
GO:0022607 | cellular component assembly | 4 | 5 |
GO:0043933 | protein-containing complex organization | 4 | 5 |
GO:0065003 | protein-containing complex assembly | 5 | 5 |
GO:0070070 | proton-transporting V-type ATPase complex assembly | 7 | 5 |
GO:0070071 | proton-transporting two-sector ATPase complex assembly | 6 | 5 |
GO:0070072 | vacuolar proton-transporting V-type ATPase complex assembly | 8 | 5 |
GO:0071840 | cellular component organization or biogenesis | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.710 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.444 |
DEG_SCF_FBW7_1 | 18 | 24 | PF00400 | 0.722 |
DEG_SCF_FBW7_1 | 34 | 41 | PF00400 | 0.617 |
DEG_SCF_TRCP1_1 | 59 | 65 | PF00400 | 0.698 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.802 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.721 |
DOC_MAPK_MEF2A_6 | 176 | 184 | PF00069 | 0.379 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.364 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.604 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.672 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.610 |
LIG_EVH1_1 | 9 | 13 | PF00568 | 0.607 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.283 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.704 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.609 |
LIG_GBD_Chelix_1 | 169 | 177 | PF00786 | 0.282 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.627 |
LIG_NRP_CendR_1 | 227 | 230 | PF00754 | 0.511 |
LIG_PCNA_yPIPBox_3 | 142 | 156 | PF02747 | 0.581 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.573 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.580 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 197 | 204 | PF11976 | 0.233 |
LIG_TYR_ITIM | 206 | 211 | PF00017 | 0.248 |
MOD_CDK_SPK_2 | 40 | 45 | PF00069 | 0.702 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.815 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.676 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.783 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.664 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.406 |
MOD_GlcNHglycan | 54 | 58 | PF01048 | 0.513 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.498 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.533 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.246 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.767 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.462 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.680 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.791 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.705 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.758 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.624 |
MOD_N-GLC_1 | 135 | 140 | PF02516 | 0.480 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.465 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.522 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.715 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.300 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.337 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.646 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.691 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.684 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.694 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.641 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.691 |
MOD_Plk_2-3 | 104 | 110 | PF00069 | 0.655 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.401 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.583 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.783 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.641 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.641 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 118 | 121 | PF00179 | 0.610 |
TRG_DiLeu_BaEn_4 | 81 | 87 | PF01217 | 0.534 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.552 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.603 |
TRG_ER_diLys_1 | 227 | 230 | PF00400 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 73 | 77 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 92 | 96 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVK4 | Leptomonas seymouri | 55% | 100% |
A0A3Q8IFH5 | Leishmania donovani | 87% | 100% |
A0A422NK67 | Trypanosoma rangeli | 37% | 100% |
A4HN91 | Leishmania braziliensis | 70% | 100% |
A4IBV9 | Leishmania infantum | 85% | 100% |
C9ZYQ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B6U9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |