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: E9AK08
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.658 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.391 |
DOC_CKS1_1 | 182 | 187 | PF01111 | 0.638 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 257 | 266 | PF00069 | 0.524 |
DOC_MAPK_gen_1 | 51 | 57 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 257 | 266 | PF00069 | 0.524 |
DOC_MAPK_NFAT4_5 | 259 | 267 | PF00069 | 0.529 |
DOC_PP2B_LxvP_1 | 3 | 6 | PF13499 | 0.465 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.682 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.564 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.479 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.757 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.589 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.589 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.400 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.711 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.457 |
LIG_PCNA_PIPBox_1 | 132 | 141 | PF02747 | 0.517 |
LIG_PCNA_yPIPBox_3 | 130 | 139 | PF02747 | 0.472 |
LIG_PCNA_yPIPBox_3 | 87 | 101 | PF02747 | 0.654 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.452 |
LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.534 |
LIG_SH2_SRC | 60 | 63 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.529 |
LIG_SH2_STAT3 | 22 | 25 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.406 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.394 |
MOD_CDK_SPxxK_3 | 188 | 195 | PF00069 | 0.525 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.630 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.652 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.753 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.672 |
MOD_Cter_Amidation | 249 | 252 | PF01082 | 0.550 |
MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.686 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.656 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.561 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.755 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.354 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.709 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.613 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.544 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.438 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.550 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.717 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.551 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.487 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.636 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.602 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.629 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.485 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.561 |
MOD_SUMO_rev_2 | 254 | 262 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 47 | 53 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_1 | 124 | 129 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_4 | 124 | 130 | PF01217 | 0.550 |
TRG_DiLeu_BaEn_4 | 133 | 139 | PF01217 | 0.358 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZG7 | Leptomonas seymouri | 53% | 86% |
A0A0S4J1V3 | Bodo saltans | 31% | 100% |
A0A1X0NLP6 | Trypanosomatidae | 33% | 100% |
A0A3R7L3M0 | Trypanosoma rangeli | 30% | 100% |
A0A3S5H590 | Leishmania donovani | 91% | 100% |
A4H3U6 | Leishmania braziliensis | 73% | 100% |
A4HS21 | Leishmania infantum | 91% | 100% |
C9ZY14 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q9XZY6 | Leishmania major | 91% | 100% |