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 |
Related structures:
AlphaFold database: A0A3S5H7F4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.575 |
CLV_Separin_Metazoa | 135 | 139 | PF03568 | 0.546 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.560 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.559 |
DEG_SPOP_SBC_1 | 230 | 234 | PF00917 | 0.660 |
DOC_MAPK_gen_1 | 82 | 92 | PF00069 | 0.745 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.499 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.678 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.759 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.575 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 207 | 215 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 229 | 238 | PF00244 | 0.614 |
LIG_Actin_WH2_2 | 129 | 146 | PF00022 | 0.594 |
LIG_CtBP_PxDLS_1 | 221 | 225 | PF00389 | 0.585 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.605 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.755 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.709 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.716 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.419 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.762 |
LIG_Integrin_isoDGR_2 | 227 | 229 | PF01839 | 0.717 |
LIG_LIR_Gen_1 | 86 | 93 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.628 |
LIG_MAD2 | 91 | 99 | PF02301 | 0.627 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.559 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.746 |
LIG_SH3_2 | 244 | 249 | PF14604 | 0.779 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.651 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.747 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.784 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.759 |
LIG_SUMO_SIM_par_1 | 162 | 170 | PF11976 | 0.713 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.729 |
LIG_WRC_WIRS_1 | 7 | 12 | PF05994 | 0.522 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.670 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.662 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.577 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.678 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.618 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.790 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.567 |
MOD_Cter_Amidation | 70 | 73 | PF01082 | 0.641 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.636 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.599 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.704 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.591 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.517 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.616 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.572 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.704 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.691 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.781 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.720 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.564 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.559 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.552 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.618 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.567 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.426 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.527 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.675 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.567 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.730 |
MOD_PK_1 | 20 | 26 | PF00069 | 0.681 |
MOD_PKA_1 | 121 | 127 | PF00069 | 0.494 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.679 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.618 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.704 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.629 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.741 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.601 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.704 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.567 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.611 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.654 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.766 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.585 |
TRG_DiLeu_BaEn_1 | 167 | 172 | PF01217 | 0.745 |
TRG_DiLeu_BaEn_4 | 241 | 247 | PF01217 | 0.686 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.652 |
TRG_NLS_MonoExtC_3 | 247 | 252 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 245 | 252 | PF00514 | 0.659 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCS9 | Leptomonas seymouri | 45% | 99% |
A4HEL3 | Leishmania braziliensis | 62% | 100% |
A4I1U4 | Leishmania infantum | 100% | 100% |
E9AXY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q9I6 | Leishmania major | 88% | 100% |