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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HL81
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.430 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.466 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.508 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 80 | 86 | PF00134 | 0.624 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.407 |
DOC_PP2B_LxvP_1 | 112 | 115 | PF13499 | 0.557 |
DOC_PP2B_LxvP_1 | 207 | 210 | PF13499 | 0.480 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.631 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.497 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.562 |
LIG_14-3-3_CanoR_1 | 100 | 105 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 119 | 129 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 199 | 209 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 237 | 241 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 53 | 62 | PF00244 | 0.651 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.441 |
LIG_EH1_1 | 147 | 155 | PF00400 | 0.386 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.714 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.382 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.595 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.661 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.561 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.394 |
LIG_GSK3_LRP6_1 | 208 | 213 | PF00069 | 0.456 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.651 |
LIG_PCNA_PIPBox_1 | 238 | 247 | PF02747 | 0.376 |
LIG_PCNA_yPIPBox_3 | 234 | 245 | PF02747 | 0.500 |
LIG_PDZ_Class_3 | 283 | 288 | PF00595 | 0.642 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.668 |
LIG_SH3_1 | 29 | 35 | PF00018 | 0.634 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.602 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.634 |
LIG_SH3_CIN85_PxpxPR_1 | 208 | 213 | PF14604 | 0.456 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.487 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.501 |
LIG_WRC_WIRS_1 | 4 | 9 | PF05994 | 0.648 |
MOD_CDK_SPK_2 | 208 | 213 | PF00069 | 0.598 |
MOD_CDK_SPxxK_3 | 208 | 215 | PF00069 | 0.589 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.462 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.522 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.627 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.530 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.455 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.491 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.423 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.394 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.571 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.554 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.584 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.632 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.547 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.484 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.473 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.510 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.542 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.600 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.658 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.530 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.596 |
MOD_N-GLC_1 | 191 | 196 | PF02516 | 0.538 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.492 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.466 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.519 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.367 |
MOD_PKA_1 | 53 | 59 | PF00069 | 0.675 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.492 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.557 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.385 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.391 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.489 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.477 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.657 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.383 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.556 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 215 | 219 | PF00026 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 29 | 34 | PF00026 | 0.633 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IHC5 | Leishmania donovani | 66% | 100% |
A4I8Q9 | Leishmania infantum | 66% | 100% |
E9B3M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 100% |
Q4Q4G3 | Leishmania major | 67% | 100% |