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: A0A3Q8IEH7
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.680 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.479 |
CLV_Separin_Metazoa | 72 | 76 | PF03568 | 0.648 |
DOC_CDC14_PxL_1 | 197 | 205 | PF14671 | 0.544 |
DOC_CDC14_PxL_1 | 48 | 56 | PF14671 | 0.634 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.628 |
DOC_CYCLIN_yCln2_LP_2 | 170 | 176 | PF00134 | 0.703 |
DOC_MAPK_MEF2A_6 | 222 | 229 | PF00069 | 0.622 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.712 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.716 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.807 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.831 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.667 |
LIG_APCC_ABBA_1 | 197 | 202 | PF00400 | 0.619 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.605 |
LIG_BIR_III_2 | 37 | 41 | PF00653 | 0.715 |
LIG_BIR_III_4 | 239 | 243 | PF00653 | 0.619 |
LIG_EH1_1 | 67 | 75 | PF00400 | 0.535 |
LIG_eIF4E_1 | 16 | 22 | PF01652 | 0.665 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.527 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.486 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.592 |
LIG_LIR_Gen_1 | 191 | 201 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.742 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.756 |
LIG_LYPXL_S_1 | 199 | 203 | PF13949 | 0.540 |
LIG_LYPXL_yS_3 | 200 | 203 | PF13949 | 0.549 |
LIG_PCNA_yPIPBox_3 | 60 | 74 | PF02747 | 0.677 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.668 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.507 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.731 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.667 |
LIG_SUMO_SIM_par_1 | 293 | 300 | PF11976 | 0.511 |
LIG_TRAF2_1 | 43 | 46 | PF00917 | 0.585 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.663 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.533 |
MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.822 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.646 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.786 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.636 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.558 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.598 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.684 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.732 |
MOD_GlcNHglycan | 151 | 155 | PF01048 | 0.631 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.702 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.705 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.647 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.517 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.527 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.496 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.681 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.571 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.721 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.700 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.745 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.641 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.634 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.650 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.677 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.457 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.684 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.632 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.777 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.392 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.616 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.536 |
MOD_NEK2_2 | 242 | 247 | PF00069 | 0.486 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.820 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.526 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.558 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.621 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.774 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.549 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.667 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.690 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.634 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.832 |
TRG_DiLeu_BaEn_1 | 259 | 264 | PF01217 | 0.697 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.549 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.680 |
TRG_NES_CRM1_1 | 280 | 293 | PF08389 | 0.475 |
TRG_NLS_MonoCore_2 | 124 | 129 | PF00514 | 0.720 |
TRG_NLS_MonoExtN_4 | 123 | 130 | PF00514 | 0.759 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYT7 | Leptomonas seymouri | 37% | 94% |
A4HCS0 | Leishmania braziliensis | 71% | 100% |
A4I094 | Leishmania infantum | 100% | 100% |
E9ACS4 | Leishmania major | 88% | 100% |
E9AW58 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |