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: E9B655
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 204 | 210 | PF00089 | 0.598 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.575 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 129 | 131 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 206 | 208 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.571 |
CLV_Separin_Metazoa | 155 | 159 | PF03568 | 0.697 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.597 |
LIG_14-3-3_CanoR_1 | 128 | 135 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.578 |
LIG_Actin_WH2_2 | 191 | 208 | PF00022 | 0.431 |
LIG_BIR_III_4 | 82 | 86 | PF00653 | 0.588 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.552 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.492 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.619 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.630 |
LIG_NRBOX | 200 | 206 | PF00104 | 0.602 |
LIG_PCNA_PIPBox_1 | 115 | 124 | PF02747 | 0.678 |
LIG_PCNA_yPIPBox_3 | 110 | 122 | PF02747 | 0.684 |
LIG_PCNA_yPIPBox_3 | 169 | 178 | PF02747 | 0.535 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.683 |
LIG_SH2_NCK_1 | 19 | 23 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 152 | 156 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.563 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 153 | 159 | PF11976 | 0.695 |
MOD_CDK_SPxK_1 | 34 | 40 | PF00069 | 0.611 |
MOD_CDK_SPxxK_3 | 41 | 48 | PF00069 | 0.618 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.673 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.616 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.662 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.643 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.501 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.671 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.677 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.555 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.648 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.692 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.689 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.616 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.555 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.562 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.561 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.611 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 133 | 136 | PF00179 | 0.718 |
MOD_SUMO_rev_2 | 123 | 127 | PF00179 | 0.650 |
MOD_SUMO_rev_2 | 78 | 86 | PF00179 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 200 | 205 | PF01217 | 0.641 |
TRG_ER_diArg_1 | 180 | 182 | PF00400 | 0.571 |
TRG_NLS_MonoExtN_4 | 126 | 132 | PF00514 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4T0 | Leptomonas seymouri | 79% | 100% |
A0A0S4KLR7 | Bodo saltans | 57% | 100% |
A0A1X0P7A8 | Trypanosomatidae | 63% | 100% |
A0A3Q8IG68 | Leishmania donovani | 97% | 100% |
A4HMJ9 | Leishmania braziliensis | 88% | 100% |
A4IB78 | Leishmania infantum | 97% | 100% |
C9ZZK2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9AEZ9 | Leishmania major | 97% | 100% |