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: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A4H7T2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.437 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.491 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.695 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.546 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.493 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.594 |
DOC_CYCLIN_RxL_1 | 74 | 85 | PF00134 | 0.623 |
DOC_PP1_RVXF_1 | 75 | 82 | PF00149 | 0.487 |
DOC_PP2B_LxvP_1 | 115 | 118 | PF13499 | 0.625 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 222 | 231 | PF00244 | 0.497 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.593 |
LIG_BIR_III_2 | 243 | 247 | PF00653 | 0.454 |
LIG_BIR_III_4 | 232 | 236 | PF00653 | 0.464 |
LIG_CAP-Gly_1 | 275 | 278 | PF01302 | 0.674 |
LIG_deltaCOP1_diTrp_1 | 22 | 31 | PF00928 | 0.493 |
LIG_eIF4E_1 | 15 | 21 | PF01652 | 0.429 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.581 |
LIG_EVH1_2 | 67 | 71 | PF00568 | 0.511 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.501 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.600 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.546 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.601 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.493 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.553 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.608 |
LIG_LIR_Apic_2 | 203 | 209 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.553 |
LIG_MYND_1 | 209 | 213 | PF01753 | 0.675 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.535 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.530 |
LIG_SH2_GRB2like | 109 | 112 | PF00017 | 0.678 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.558 |
LIG_WW_3 | 207 | 211 | PF00397 | 0.671 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.530 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.537 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.714 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.600 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.444 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.513 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.572 |
MOD_GlcNHglycan | 155 | 160 | PF01048 | 0.552 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.523 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.775 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.745 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.570 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.621 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.529 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.644 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.608 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.499 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.649 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.390 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.425 |
MOD_N-GLC_1 | 137 | 142 | PF02516 | 0.645 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.516 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.461 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.525 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.548 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.569 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.713 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.502 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.579 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.385 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.697 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.539 |
MOD_PK_1 | 227 | 233 | PF00069 | 0.553 |
MOD_PKB_1 | 220 | 228 | PF00069 | 0.574 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.516 |
MOD_Plk_1 | 46 | 52 | PF00069 | 0.607 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.492 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.468 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.473 |
TRG_DiLeu_BaEn_1 | 219 | 224 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.581 |
TRG_DiLeu_LyEn_5 | 219 | 224 | PF01217 | 0.571 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P396 | Leptomonas seymouri | 65% | 97% |
A0A0S4J125 | Bodo saltans | 33% | 100% |
A0A0S4J4Y9 | Bodo saltans | 32% | 100% |
A0A1X0P9Q3 | Trypanosomatidae | 40% | 100% |
A0A3Q8IH55 | Leishmania donovani | 81% | 100% |
A0A3R7LYE4 | Trypanosoma rangeli | 41% | 100% |
A4I9V4 | Leishmania infantum | 81% | 100% |
C9ZMS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B4W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q360 | Leishmania major | 81% | 100% |
V5DJW1 | Trypanosoma cruzi | 37% | 96% |