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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HC62
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.577 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.677 |
DOC_MAPK_gen_1 | 177 | 183 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.551 |
DOC_MAPK_RevD_3 | 163 | 178 | PF00069 | 0.539 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 167 | 170 | PF00568 | 0.651 |
DOC_SPAK_OSR1_1 | 33 | 37 | PF12202 | 0.626 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.690 |
DOC_USP7_UBL2_3 | 137 | 141 | PF12436 | 0.354 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 211 | 219 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.602 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.470 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.636 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.612 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.631 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.517 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.462 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.667 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.410 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.473 |
LIG_LIR_Gen_1 | 128 | 136 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.562 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 117 | 120 | PF00017 | 0.607 |
LIG_SH2_STAT3 | 179 | 182 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.553 |
LIG_SUMO_SIM_anti_2 | 96 | 103 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.462 |
LIG_WRC_WIRS_1 | 198 | 203 | PF05994 | 0.545 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.614 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.723 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.482 |
MOD_Cter_Amidation | 19 | 22 | PF01082 | 0.647 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.475 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.517 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.574 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.567 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.616 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.619 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.575 |
MOD_LATS_1 | 209 | 215 | PF00433 | 0.626 |
MOD_LATS_1 | 82 | 88 | PF00433 | 0.425 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.498 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.461 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.511 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.497 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.660 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.631 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.589 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.505 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.557 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.462 |
MOD_NEK2_2 | 230 | 235 | PF00069 | 0.641 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.610 |
MOD_PK_1 | 177 | 183 | PF00069 | 0.525 |
MOD_PK_1 | 93 | 99 | PF00069 | 0.605 |
MOD_PKA_1 | 177 | 183 | PF00069 | 0.584 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.572 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.584 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.612 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.534 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.507 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.424 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.572 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.585 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.437 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.552 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.600 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.460 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.370 |
MOD_SUMO_for_1 | 80 | 83 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_2 | 73 | 79 | PF01217 | 0.616 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.612 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZN5 | Leptomonas seymouri | 62% | 100% |
A0A1X0NTR1 | Trypanosomatidae | 38% | 82% |
A0A3Q8IC30 | Leishmania donovani | 76% | 100% |
A0A3R7LNK0 | Trypanosoma rangeli | 33% | 89% |
C9ZSC5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
E9AGZ0 | Leishmania infantum | 75% | 100% |
E9AVJ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4QBY4 | Leishmania major | 76% | 100% |
V5BFS1 | Trypanosoma cruzi | 30% | 87% |