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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HMS8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.458 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.780 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.804 |
CLV_PCSK_PC7_1 | 191 | 197 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.693 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.511 |
CLV_Separin_Metazoa | 12 | 16 | PF03568 | 0.471 |
DOC_CKS1_1 | 79 | 84 | PF01111 | 0.663 |
DOC_CYCLIN_RxL_1 | 164 | 176 | PF00134 | 0.786 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.480 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.534 |
DOC_WW_Pin1_4 | 118 | 123 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 148 | 153 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 173 | 180 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 200 | 209 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 95 | 101 | PF00244 | 0.541 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.512 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.544 |
LIG_DLG_GKlike_1 | 148 | 155 | PF00625 | 0.522 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.722 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.724 |
LIG_LIR_Apic_2 | 129 | 135 | PF02991 | 0.549 |
LIG_SH3_1 | 164 | 170 | PF00018 | 0.534 |
LIG_SH3_2 | 79 | 84 | PF14604 | 0.663 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.596 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.626 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.738 |
LIG_SUMO_SIM_anti_2 | 32 | 39 | PF11976 | 0.629 |
LIG_SUMO_SIM_anti_2 | 54 | 60 | PF11976 | 0.532 |
MOD_CDC14_SPxK_1 | 91 | 94 | PF00782 | 0.705 |
MOD_CDK_SPxK_1 | 78 | 84 | PF00069 | 0.664 |
MOD_CDK_SPxK_1 | 88 | 94 | PF00069 | 0.710 |
MOD_CDK_SPxxK_3 | 157 | 164 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 88 | 95 | PF00069 | 0.711 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.634 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.693 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.665 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.793 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.550 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.532 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.756 |
MOD_Cter_Amidation | 188 | 191 | PF01082 | 0.554 |
MOD_Cter_Amidation | 59 | 62 | PF01082 | 0.489 |
MOD_DYRK1A_RPxSP_1 | 78 | 82 | PF00069 | 0.692 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.744 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.697 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.789 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.675 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.761 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.705 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.643 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.788 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.768 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.704 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.557 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.722 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.745 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.543 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.715 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.712 |
MOD_PK_1 | 202 | 208 | PF00069 | 0.723 |
MOD_PK_1 | 84 | 90 | PF00069 | 0.785 |
MOD_PKA_1 | 194 | 200 | PF00069 | 0.720 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.734 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.727 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.755 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.500 |
MOD_PKB_1 | 113 | 121 | PF00069 | 0.618 |
MOD_PKB_1 | 194 | 202 | PF00069 | 0.733 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.555 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.558 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.538 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.639 |
MOD_ProDKin_1 | 118 | 124 | PF00069 | 0.686 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.703 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.647 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.664 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.710 |
TRG_DiLeu_BaEn_3 | 32 | 38 | PF01217 | 0.377 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.720 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.800 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 200 | 202 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.684 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P940 | Leptomonas seymouri | 58% | 100% |
A0A3S7X9C5 | Leishmania donovani | 75% | 100% |
A4IBG6 | Leishmania infantum | 75% | 100% |
C9ZZ99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AF80 | Leishmania major | 74% | 100% |
E9B6D6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |