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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A0A3Q8IBZ4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.671 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.812 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.695 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.812 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 128 | 134 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.513 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.649 |
DOC_CYCLIN_yCln2_LP_2 | 15 | 21 | PF00134 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 73 | 76 | PF00134 | 0.589 |
DOC_MAPK_MEF2A_6 | 214 | 221 | PF00069 | 0.763 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.589 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.619 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 13 | 18 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 41 | 49 | PF00244 | 0.396 |
LIG_BIR_III_4 | 165 | 169 | PF00653 | 0.705 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.702 |
LIG_EVH1_1 | 74 | 78 | PF00568 | 0.612 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.513 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.642 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.626 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.614 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.700 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.498 |
LIG_MYND_1 | 98 | 102 | PF01753 | 0.778 |
LIG_SH2_STAT3 | 9 | 12 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.664 |
LIG_SH3_2 | 98 | 103 | PF14604 | 0.703 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.738 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.605 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.655 |
LIG_SUMO_SIM_anti_2 | 55 | 60 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.656 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.698 |
LIG_WW_2 | 75 | 78 | PF00397 | 0.629 |
LIG_WW_3 | 100 | 104 | PF00397 | 0.770 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.737 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.678 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.722 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.693 |
MOD_Cter_Amidation | 179 | 182 | PF01082 | 0.655 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.777 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.632 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.803 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.805 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.812 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.795 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.665 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.411 |
MOD_PKA_1 | 121 | 127 | PF00069 | 0.812 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.622 |
MOD_PKA_1 | 141 | 147 | PF00069 | 0.485 |
MOD_PKA_1 | 182 | 188 | PF00069 | 0.802 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.771 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.639 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.485 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.723 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.398 |
MOD_PKB_1 | 132 | 140 | PF00069 | 0.768 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.740 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.618 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.712 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.657 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.631 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.708 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 140 | 142 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4B1 | Leptomonas seymouri | 46% | 100% |
A4H7M0 | Leishmania braziliensis | 68% | 99% |
A4HW05 | Leishmania infantum | 99% | 100% |
E9APQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QFS2 | Leishmania major | 89% | 100% |