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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A451EJS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 178 | 182 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.569 |
CLV_PCSK_FUR_1 | 300 | 304 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.579 |
CLV_Separin_Metazoa | 128 | 132 | PF03568 | 0.545 |
DEG_APCC_DBOX_1 | 156 | 164 | PF00400 | 0.597 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.523 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.600 |
DOC_MAPK_gen_1 | 220 | 228 | PF00069 | 0.568 |
DOC_MAPK_MEF2A_6 | 203 | 212 | PF00069 | 0.429 |
DOC_MAPK_NFAT4_5 | 209 | 217 | PF00069 | 0.367 |
DOC_MAPK_RevD_3 | 206 | 221 | PF00069 | 0.486 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.653 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.522 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.584 |
DOC_USP7_UBL2_3 | 37 | 41 | PF12436 | 0.669 |
DOC_USP7_UBL2_3 | 94 | 98 | PF12436 | 0.465 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.418 |
LIG_14-3-3_CanoR_1 | 203 | 210 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 220 | 224 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.671 |
LIG_Actin_WH2_1 | 209 | 226 | PF00022 | 0.436 |
LIG_Actin_WH2_2 | 210 | 226 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 56 | 61 | PF00400 | 0.547 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.586 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.586 |
LIG_BIR_III_2 | 349 | 353 | PF00653 | 0.540 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.586 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.528 |
LIG_deltaCOP1_diTrp_1 | 169 | 174 | PF00928 | 0.537 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.555 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.537 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.539 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.460 |
LIG_LIR_Apic_2 | 173 | 177 | PF02991 | 0.581 |
LIG_LIR_Apic_2 | 370 | 376 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 237 | 248 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.509 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.505 |
LIG_SH2_PTP2 | 377 | 380 | PF00017 | 0.557 |
LIG_SH2_SRC | 110 | 113 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 238 | 241 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 377 | 380 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.438 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.507 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.525 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.646 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.688 |
LIG_TRAF2_1 | 121 | 124 | PF00917 | 0.520 |
LIG_TRAF2_1 | 309 | 312 | PF00917 | 0.490 |
MOD_CDC14_SPxK_1 | 353 | 356 | PF00782 | 0.523 |
MOD_CDK_SPxK_1 | 350 | 356 | PF00069 | 0.532 |
MOD_CDK_SPxK_1 | 394 | 400 | PF00069 | 0.567 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.569 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.645 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.488 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.626 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.609 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.511 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.545 |
MOD_CMANNOS | 171 | 174 | PF00535 | 0.535 |
MOD_Cter_Amidation | 23 | 26 | PF01082 | 0.599 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.560 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.605 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.531 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.655 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.415 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.566 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.587 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.656 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.597 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.615 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.641 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.767 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.603 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.579 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.660 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.455 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.619 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.705 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.657 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.589 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.548 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.387 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.597 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.595 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.637 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.662 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.403 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.527 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.669 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.582 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.472 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.677 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.647 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.575 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.390 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.468 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.457 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.567 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.647 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.474 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.547 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.628 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.570 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.482 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.479 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.466 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.630 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.573 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.694 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.591 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.662 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.454 |
MOD_SUMO_for_1 | 93 | 96 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 152 | 160 | PF00179 | 0.568 |
MOD_SUMO_rev_2 | 190 | 200 | PF00179 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 389 | 394 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 299 | 302 | PF00400 | 0.589 |
TRG_NES_CRM1_1 | 260 | 274 | PF08389 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBW0 | Leptomonas seymouri | 42% | 84% |
A0A3R7KL86 | Trypanosoma rangeli | 24% | 100% |
A4H3N4 | Leishmania braziliensis | 63% | 100% |
A4HRW1 | Leishmania infantum | 100% | 100% |
C9ZKG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
E9ACL8 | Leishmania major | 91% | 99% |
E9AJV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |