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: A4HBQ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.573 |
CLV_PCSK_FUR_1 | 345 | 349 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 347 | 349 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 363 | 365 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.753 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.509 |
DOC_CYCLIN_yCln2_LP_2 | 65 | 71 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 263 | 272 | PF00069 | 0.754 |
DOC_PP2B_LxvP_1 | 240 | 243 | PF13499 | 0.600 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.527 |
DOC_PP4_FxxP_1 | 183 | 186 | PF00568 | 0.519 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.557 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.626 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.763 |
LIG_14-3-3_CanoR_1 | 207 | 215 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 226 | 231 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 263 | 268 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 303 | 313 | PF00244 | 0.817 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.555 |
LIG_BRCT_BRCA1_1 | 179 | 183 | PF00533 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 97 | 105 | PF00928 | 0.546 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.755 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.574 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.775 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.757 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.511 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.584 |
LIG_Integrin_RGD_1 | 348 | 350 | PF01839 | 0.519 |
LIG_LIR_Apic_2 | 180 | 186 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 307 | 313 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 97 | 103 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 368 | 374 | PF02991 | 0.729 |
LIG_LYPXL_yS_3 | 250 | 253 | PF13949 | 0.649 |
LIG_NRP_CendR_1 | 378 | 381 | PF00754 | 0.742 |
LIG_SH2_PTP2 | 167 | 170 | PF00017 | 0.507 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.721 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.819 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.675 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.585 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.648 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.673 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.642 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.563 |
LIG_SUMO_SIM_par_1 | 243 | 248 | PF11976 | 0.645 |
LIG_TYR_ITSM | 246 | 253 | PF00017 | 0.651 |
MOD_CDK_SPxxK_3 | 296 | 303 | PF00069 | 0.568 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.729 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.554 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.563 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.583 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.489 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.567 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.683 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.771 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.751 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.832 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.645 |
MOD_Cter_Amidation | 224 | 227 | PF01082 | 0.478 |
MOD_Cter_Amidation | 376 | 379 | PF01082 | 0.615 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.671 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.638 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.630 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.550 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.489 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.697 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.784 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.795 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.795 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.769 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.593 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.538 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.822 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.518 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.615 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.768 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.534 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.562 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.677 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.704 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.505 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.812 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.804 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.598 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.815 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.527 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.536 |
MOD_NEK2_2 | 352 | 357 | PF00069 | 0.497 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.439 |
MOD_PKA_1 | 263 | 269 | PF00069 | 0.759 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.543 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.723 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.597 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.597 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.657 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.727 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.716 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.612 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.567 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.511 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.460 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.764 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.677 |
TRG_ENDOCYTIC_2 | 250 | 253 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.632 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.730 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8I5 | Leptomonas seymouri | 42% | 80% |
A0A3S7WWD4 | Leishmania donovani | 65% | 98% |
A4HZ58 | Leishmania infantum | 65% | 98% |
E9AV26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 99% |
Q4QCF6 | Leishmania major | 65% | 100% |