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: Q4Q9I6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.621 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.472 |
CLV_Separin_Metazoa | 135 | 139 | PF03568 | 0.445 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.454 |
DEG_SPOP_SBC_1 | 221 | 225 | PF00917 | 0.629 |
DOC_MAPK_gen_1 | 82 | 92 | PF00069 | 0.627 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.579 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.494 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.567 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.637 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.472 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.789 |
LIG_14-3-3_CanoR_1 | 115 | 124 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.605 |
LIG_Actin_WH2_2 | 129 | 146 | PF00022 | 0.499 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.528 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.572 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.590 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.528 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.538 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.650 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.401 |
LIG_Integrin_isoDGR_2 | 228 | 230 | PF01839 | 0.644 |
LIG_LIR_Gen_1 | 86 | 93 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.552 |
LIG_MAD2 | 91 | 99 | PF02301 | 0.550 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.454 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.677 |
LIG_SH3_2 | 245 | 250 | PF14604 | 0.640 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.662 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.738 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.585 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.667 |
LIG_SH3_CIN85_PxpxPR_1 | 194 | 199 | PF14604 | 0.505 |
LIG_SUMO_SIM_par_1 | 163 | 171 | PF11976 | 0.553 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.618 |
LIG_WRC_WIRS_1 | 7 | 12 | PF05994 | 0.468 |
LIG_WW_3 | 122 | 126 | PF00397 | 0.486 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.570 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.516 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.559 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.624 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.514 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.683 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.518 |
MOD_Cter_Amidation | 70 | 73 | PF01082 | 0.545 |
MOD_DYRK1A_RPxSP_1 | 230 | 234 | PF00069 | 0.561 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.570 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.549 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.581 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.759 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.636 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.528 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.688 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.723 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.594 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.619 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.463 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.528 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.597 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.667 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.439 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.470 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.507 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.461 |
MOD_PK_1 | 20 | 26 | PF00069 | 0.584 |
MOD_PK_1 | 208 | 214 | PF00069 | 0.524 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.599 |
MOD_PKA_1 | 249 | 255 | PF00069 | 0.514 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.614 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.549 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.642 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.623 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.461 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.520 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.448 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.480 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.709 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.787 |
TRG_DiLeu_BaEn_1 | 168 | 173 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_4 | 242 | 248 | PF01217 | 0.591 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.599 |
TRG_NLS_MonoExtC_3 | 248 | 253 | PF00514 | 0.528 |
TRG_NLS_MonoExtN_4 | 246 | 253 | PF00514 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCS9 | Leptomonas seymouri | 44% | 99% |
A0A3S5H7F4 | Leishmania donovani | 88% | 100% |
A4HEL3 | Leishmania braziliensis | 59% | 100% |
A4I1U4 | Leishmania infantum | 88% | 100% |
E9AXY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |