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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S5H5I0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 199 | 203 | PF00656 | 0.453 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.531 |
CLV_PCSK_FUR_1 | 189 | 193 | PF00082 | 0.485 |
CLV_PCSK_FUR_1 | 227 | 231 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.494 |
CLV_Separin_Metazoa | 214 | 218 | PF03568 | 0.529 |
DEG_APCC_DBOX_1 | 190 | 198 | PF00400 | 0.487 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.611 |
DOC_CYCLIN_RxL_1 | 188 | 200 | PF00134 | 0.507 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 124 | 130 | PF00134 | 0.599 |
DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 190 | 197 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.631 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.795 |
LIG_14-3-3_CanoR_1 | 107 | 114 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 143 | 152 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.561 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.556 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.617 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.637 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.476 |
LIG_GBD_Chelix_1 | 13 | 21 | PF00786 | 0.474 |
LIG_MYND_1 | 123 | 127 | PF01753 | 0.556 |
LIG_MYND_1 | 135 | 139 | PF01753 | 0.551 |
LIG_SH2_CRK | 31 | 35 | PF00017 | 0.507 |
LIG_SH2_GRB2like | 204 | 207 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.446 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.650 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.511 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.642 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.579 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.539 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.600 |
MOD_CDK_SPxxK_3 | 135 | 142 | PF00069 | 0.550 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.557 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.639 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.590 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.486 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.538 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.582 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.703 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.599 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.560 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.552 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.590 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.595 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.621 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.489 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.562 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.528 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.549 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.551 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.590 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.575 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.604 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.510 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.793 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 120 | 125 | PF01217 | 0.527 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.651 |
TRG_NLS_Bipartite_1 | 210 | 228 | PF00514 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZW8 | Leptomonas seymouri | 34% | 100% |
A4H493 | Leishmania braziliensis | 60% | 82% |
A4HSG9 | Leishmania infantum | 100% | 100% |
E9AKF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QJF5 | Leishmania major | 90% | 100% |