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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3S5H557
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.584 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.436 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.621 |
CLV_Separin_Metazoa | 268 | 272 | PF03568 | 0.502 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.396 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.621 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.564 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.568 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.745 |
DOC_CKS1_1 | 167 | 172 | PF01111 | 0.440 |
DOC_MAPK_gen_1 | 87 | 94 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.385 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.671 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.725 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.475 |
LIG_CtBP_PxDLS_1 | 177 | 181 | PF00389 | 0.406 |
LIG_eIF4E_1 | 113 | 119 | PF01652 | 0.419 |
LIG_EVH1_1 | 76 | 80 | PF00568 | 0.611 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.633 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.530 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.466 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.521 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.531 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.682 |
LIG_Integrin_RGD_1 | 36 | 38 | PF01839 | 0.596 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.586 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.453 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.600 |
LIG_SH2_PTP2 | 252 | 255 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.455 |
LIG_SH3_2 | 49 | 54 | PF14604 | 0.600 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.361 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.364 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.729 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.569 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.488 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.676 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.676 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.423 |
LIG_SxIP_EBH_1 | 16 | 26 | PF03271 | 0.539 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.636 |
LIG_WW_3 | 58 | 62 | PF00397 | 0.629 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.628 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.526 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.679 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.692 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.538 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.567 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.597 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.479 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.614 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.653 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.610 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.697 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.489 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.585 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.622 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.637 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.623 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.609 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.319 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.678 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.479 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.295 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.581 |
MOD_PK_1 | 260 | 266 | PF00069 | 0.527 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.720 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.412 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.483 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.715 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.646 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.724 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.605 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.336 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.749 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.619 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.688 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 281 | 288 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.514 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCN8 | Leptomonas seymouri | 58% | 95% |
A0A1X0PA92 | Trypanosomatidae | 39% | 100% |
A0A3R7KEM6 | Trypanosoma rangeli | 41% | 100% |
A4HRW4 | Leishmania infantum | 99% | 100% |
C9ZKG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ACM1 | Leishmania major | 91% | 100% |
E9AJV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
V5BC94 | Trypanosoma cruzi | 40% | 100% |