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: A4HMJ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.537 |
CLV_Separin_Metazoa | 154 | 158 | PF03568 | 0.632 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.530 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.540 |
LIG_14-3-3_CanoR_1 | 127 | 137 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 190 | 207 | PF00022 | 0.399 |
LIG_BIR_III_4 | 81 | 85 | PF00653 | 0.520 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.654 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.457 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.423 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.615 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.619 |
LIG_NRBOX | 199 | 205 | PF00104 | 0.572 |
LIG_PCNA_PIPBox_1 | 114 | 123 | PF02747 | 0.609 |
LIG_PCNA_yPIPBox_3 | 109 | 121 | PF02747 | 0.607 |
LIG_PCNA_yPIPBox_3 | 168 | 177 | PF02747 | 0.510 |
LIG_Pex14_2 | 48 | 52 | PF04695 | 0.627 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.490 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.587 |
LIG_SUMO_SIM_anti_2 | 152 | 158 | PF11976 | 0.630 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.436 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.409 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.572 |
MOD_CDK_SPxK_1 | 33 | 39 | PF00069 | 0.610 |
MOD_CDK_SPxxK_3 | 40 | 47 | PF00069 | 0.556 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.671 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.495 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.614 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.407 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.625 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.596 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.526 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.645 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.391 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.609 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.554 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.622 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.522 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.479 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.483 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.493 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.610 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.533 |
MOD_SUMO_rev_2 | 77 | 85 | PF00179 | 0.492 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4T0 | Leptomonas seymouri | 79% | 100% |
A0A0S4KLR7 | Bodo saltans | 61% | 100% |
A0A1X0P7A8 | Trypanosomatidae | 62% | 100% |
A0A3Q8IG68 | Leishmania donovani | 87% | 100% |
A4IB78 | Leishmania infantum | 87% | 100% |
C9ZZK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AEZ9 | Leishmania major | 87% | 100% |
E9B655 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |