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: A4HID0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.442 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.706 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.355 |
DEG_APCC_DBOX_1 | 173 | 181 | PF00400 | 0.524 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.386 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 134 | 143 | PF00134 | 0.491 |
DOC_MAPK_MEF2A_6 | 172 | 180 | PF00069 | 0.531 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.525 |
DOC_PP1_RVXF_1 | 402 | 408 | PF00149 | 0.499 |
DOC_SPAK_OSR1_1 | 163 | 167 | PF12202 | 0.635 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.296 |
LIG_14-3-3_CanoR_1 | 212 | 221 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 238 | 246 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 265 | 275 | PF00244 | 0.600 |
LIG_Actin_WH2_2 | 380 | 397 | PF00022 | 0.518 |
LIG_APCC_ABBA_1 | 83 | 88 | PF00400 | 0.238 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.547 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.533 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.488 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.355 |
LIG_CtBP_PxDLS_1 | 131 | 135 | PF00389 | 0.506 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.550 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.524 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.355 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.636 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.550 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.664 |
LIG_LIR_Apic_2 | 145 | 151 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.273 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.238 |
LIG_Pex14_2 | 199 | 203 | PF04695 | 0.508 |
LIG_Pex14_2 | 313 | 317 | PF04695 | 0.511 |
LIG_Pex14_2 | 86 | 90 | PF04695 | 0.355 |
LIG_REV1ctd_RIR_1 | 296 | 304 | PF16727 | 0.507 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.651 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.238 |
LIG_SH2_STAT3 | 153 | 156 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.296 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.517 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.490 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.477 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.499 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.229 |
LIG_SUMO_SIM_anti_2 | 102 | 111 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.465 |
LIG_UBA3_1 | 106 | 113 | PF00899 | 0.405 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.567 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.546 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.604 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.571 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.740 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.601 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.541 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.553 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.588 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.535 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.557 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.522 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.489 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.548 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.594 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.645 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.455 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.493 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.544 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.649 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.555 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.574 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.562 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.556 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.441 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.702 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.524 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.585 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.526 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.590 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.518 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.541 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.622 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.696 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.550 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.516 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.355 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.540 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.533 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.486 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.499 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.607 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.732 |
MOD_PKB_1 | 386 | 394 | PF00069 | 0.398 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.438 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.520 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.438 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.543 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.611 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.355 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.614 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.488 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.523 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.646 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.605 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.560 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.296 |
MOD_SUMO_for_1 | 352 | 355 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 389 | 397 | PF00179 | 0.408 |
TRG_DiLeu_BaEn_2 | 1 | 7 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_4 | 389 | 395 | PF01217 | 0.521 |
TRG_DiLeu_BaLyEn_6 | 102 | 107 | PF01217 | 0.353 |
TRG_DiLeu_BaLyEn_6 | 241 | 246 | PF01217 | 0.518 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.388 |
TRG_ER_diArg_1 | 402 | 405 | PF00400 | 0.499 |
TRG_NES_CRM1_1 | 375 | 389 | PF08389 | 0.390 |
TRG_NLS_MonoExtN_4 | 262 | 268 | PF00514 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IML8 | Leptomonas seymouri | 31% | 92% |
A0A3Q8IEA2 | Leishmania donovani | 54% | 95% |
A4I5M3 | Leishmania infantum | 54% | 96% |
E9B0W8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 98% |