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: E9AXY8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.728 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.562 |
CLV_Separin_Metazoa | 135 | 139 | PF03568 | 0.556 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.547 |
DOC_MAPK_gen_1 | 81 | 92 | PF00069 | 0.647 |
DOC_PP2B_LxvP_1 | 219 | 222 | PF13499 | 0.514 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.599 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.672 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.754 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.774 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.763 |
LIG_Actin_WH2_2 | 129 | 146 | PF00022 | 0.606 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.637 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.607 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.683 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.628 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.722 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.504 |
LIG_LIR_Gen_1 | 86 | 93 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.640 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.548 |
LIG_PTAP_UEV_1 | 177 | 182 | PF05743 | 0.555 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.738 |
LIG_SH3_2 | 245 | 250 | PF14604 | 0.773 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.703 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.760 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.812 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.756 |
LIG_SUMO_SIM_par_1 | 163 | 171 | PF11976 | 0.702 |
LIG_WRC_WIRS_1 | 7 | 12 | PF05994 | 0.558 |
LIG_WW_3 | 122 | 126 | PF00397 | 0.542 |
MOD_CDK_SPK_2 | 241 | 246 | PF00069 | 0.518 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.672 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.510 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.631 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.616 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.606 |
MOD_Cter_Amidation | 70 | 73 | PF01082 | 0.635 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.657 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.671 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.811 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.600 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.754 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.724 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.671 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.726 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.539 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.559 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.637 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.658 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.380 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.567 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.680 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.557 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.559 |
MOD_PKA_1 | 249 | 255 | PF00069 | 0.616 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.700 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.651 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.739 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.714 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.557 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.573 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.783 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.551 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.780 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.810 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.770 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.710 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.648 |
TRG_NLS_MonoExtC_3 | 248 | 253 | PF00514 | 0.632 |
TRG_NLS_MonoExtC_3 | 80 | 85 | PF00514 | 0.461 |
TRG_NLS_MonoExtN_4 | 246 | 253 | PF00514 | 0.655 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCS9 | Leptomonas seymouri | 44% | 99% |
A0A3S5H7F4 | Leishmania donovani | 82% | 100% |
A4HEL3 | Leishmania braziliensis | 62% | 100% |
A4I1U4 | Leishmania infantum | 82% | 100% |
Q4Q9I6 | Leishmania major | 80% | 100% |