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: A4HRW4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.595 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.434 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.649 |
CLV_Separin_Metazoa | 268 | 272 | PF03568 | 0.493 |
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 | 0.573 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.553 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.729 |
DOC_CYCLIN_yCln2_LP_2 | 181 | 187 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 87 | 94 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.384 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.517 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.688 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 2 | 7 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 54 | 59 | PF00244 | 0.770 |
LIG_BRCT_BRCA1_1 | 115 | 119 | PF00533 | 0.476 |
LIG_eIF4E_1 | 113 | 119 | PF01652 | 0.427 |
LIG_EVH1_1 | 76 | 80 | PF00568 | 0.616 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.631 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.439 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.450 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.495 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.536 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.735 |
LIG_Integrin_RGD_1 | 36 | 38 | PF01839 | 0.581 |
LIG_LIR_Gen_1 | 116 | 127 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.595 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.461 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.590 |
LIG_SH2_PTP2 | 252 | 255 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.411 |
LIG_SH3_2 | 49 | 54 | PF14604 | 0.588 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.378 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.366 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.652 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.527 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.657 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.683 |
LIG_SUMO_SIM_par_1 | 260 | 265 | PF11976 | 0.397 |
LIG_SxIP_EBH_1 | 16 | 26 | PF03271 | 0.537 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.581 |
LIG_WW_3 | 58 | 62 | PF00397 | 0.626 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.594 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.517 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.672 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.631 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.534 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.444 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.602 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.479 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.622 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.652 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.582 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.648 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.502 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.616 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.670 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.626 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.622 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.608 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.324 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.677 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.461 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.502 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.538 |
MOD_PK_1 | 260 | 266 | PF00069 | 0.503 |
MOD_PKA_1 | 54 | 60 | PF00069 | 0.710 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.420 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.484 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.491 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.636 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.723 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.607 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.388 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.748 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.642 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.666 |
MOD_SUMO_for_1 | 282 | 285 | PF00179 | 0.552 |
MOD_SUMO_rev_2 | 281 | 288 | PF00179 | 0.544 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.448 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 86 | 89 | PF00400 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCN8 | Leptomonas seymouri | 66% | 95% |
A0A1X0PA92 | Trypanosomatidae | 39% | 100% |
A0A3R7KEM6 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H557 | Leishmania donovani | 99% | 100% |
C9ZKG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ACM1 | Leishmania major | 91% | 100% |
E9AJV9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
V5BC94 | Trypanosoma cruzi | 42% | 100% |