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: E9AF15
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.661 |
CLV_PCSK_FUR_1 | 108 | 112 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.705 |
CLV_Separin_Metazoa | 187 | 191 | PF03568 | 0.566 |
CLV_Separin_Metazoa | 316 | 320 | PF03568 | 0.553 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.404 |
DEG_APCC_KENBOX_2 | 408 | 412 | PF00400 | 0.665 |
DEG_SPOP_SBC_1 | 250 | 254 | PF00917 | 0.574 |
DOC_MAPK_gen_1 | 212 | 220 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 438 | 448 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 214 | 222 | PF00069 | 0.412 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.670 |
DOC_PP2B_LxvP_1 | 97 | 100 | PF13499 | 0.640 |
DOC_PP4_FxxP_1 | 340 | 343 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.618 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 364 | 369 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 380 | 384 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 63 | 73 | PF00244 | 0.547 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.577 |
LIG_BIR_III_4 | 58 | 62 | PF00653 | 0.555 |
LIG_BRCT_BRCA1_1 | 412 | 416 | PF00533 | 0.552 |
LIG_deltaCOP1_diTrp_1 | 327 | 333 | PF00928 | 0.503 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.603 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.576 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.539 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.517 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.576 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.748 |
LIG_LIR_Apic_2 | 397 | 402 | PF02991 | 0.625 |
LIG_LIR_Gen_1 | 76 | 85 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.640 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.489 |
LIG_PDZ_Class_2 | 443 | 448 | PF00595 | 0.645 |
LIG_Pex14_1 | 329 | 333 | PF04695 | 0.513 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.469 |
LIG_PTB_Apo_2 | 188 | 195 | PF02174 | 0.568 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.644 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.474 |
LIG_SH2_GRB2like | 73 | 76 | PF00017 | 0.609 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.517 |
LIG_SH2_STAT3 | 332 | 335 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.478 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.693 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.682 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.530 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.631 |
LIG_WRC_WIRS_1 | 5 | 10 | PF05994 | 0.570 |
MOD_CDC14_SPxK_1 | 248 | 251 | PF00782 | 0.690 |
MOD_CDK_SPxK_1 | 245 | 251 | PF00069 | 0.689 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.648 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.693 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.585 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.695 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.562 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.662 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.744 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.532 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.629 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.702 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.511 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.566 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.630 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.603 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.664 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.630 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.566 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.558 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.570 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.576 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.566 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.676 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.628 |
MOD_PKA_1 | 438 | 444 | PF00069 | 0.647 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.628 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.611 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.656 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.455 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.588 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.581 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.575 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.602 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.494 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.652 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.638 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.730 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.439 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.679 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.491 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.770 |
MOD_ProDKin_1 | 364 | 370 | PF00069 | 0.526 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.632 |
MOD_SUMO_for_1 | 257 | 260 | PF00179 | 0.657 |
TRG_DiLeu_BaEn_1 | 443 | 448 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_4 | 239 | 245 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.655 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.572 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.797 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZQ4 | Leptomonas seymouri | 48% | 97% |
A0A3S5H7Z2 | Leishmania donovani | 93% | 100% |
A4HML4 | Leishmania braziliensis | 77% | 100% |
A4IB91 | Leishmania infantum | 93% | 100% |
E9B671 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |