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: Q4QF24
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.441 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.615 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.668 |
DOC_MAPK_gen_1 | 142 | 150 | PF00069 | 0.577 |
DOC_PP1_RVXF_1 | 13 | 19 | PF00149 | 0.474 |
DOC_PP1_RVXF_1 | 22 | 28 | PF00149 | 0.500 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.704 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 158 | 166 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 183 | 193 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 209 | 214 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.728 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.594 |
LIG_LIR_Apic_2 | 117 | 121 | PF02991 | 0.629 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.542 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.604 |
LIG_SH2_STAT3 | 98 | 101 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.684 |
LIG_SH3_1 | 196 | 202 | PF00018 | 0.671 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.640 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.705 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.658 |
LIG_TRAF2_1 | 154 | 157 | PF00917 | 0.503 |
MOD_CDK_SPxxK_3 | 151 | 158 | PF00069 | 0.542 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.687 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.480 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.575 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.739 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.680 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.605 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.617 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.589 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.690 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.597 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.620 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.554 |
MOD_PK_1 | 209 | 215 | PF00069 | 0.702 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.635 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.429 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.613 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.487 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.542 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.634 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.680 |
TRG_NLS_Bipartite_1 | 37 | 51 | PF00514 | 0.664 |
TRG_NLS_MonoExtC_3 | 36 | 41 | PF00514 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7M0 | Leptomonas seymouri | 58% | 100% |
A0A0S4J706 | Bodo saltans | 32% | 94% |
A0A1X0NU63 | Trypanosomatidae | 36% | 96% |
A0A3R7MDP5 | Trypanosoma rangeli | 35% | 97% |
A0A3S7WTQ3 | Leishmania donovani | 93% | 100% |
A4H8C3 | Leishmania braziliensis | 81% | 74% |
A4HWP4 | Leishmania infantum | 94% | 100% |
C9ZXP2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 93% |
E9AQF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |