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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S5H694
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.554 |
CLV_Separin_Metazoa | 134 | 138 | PF03568 | 0.485 |
DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.465 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.524 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.510 |
DOC_CYCLIN_yCln2_LP_2 | 358 | 364 | PF00134 | 0.503 |
DOC_MAPK_gen_1 | 11 | 18 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.624 |
DOC_MAPK_MEF2A_6 | 141 | 150 | PF00069 | 0.433 |
DOC_MAPK_NFAT4_5 | 11 | 19 | PF00069 | 0.614 |
DOC_PP2B_LxvP_1 | 16 | 19 | PF13499 | 0.578 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.570 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.522 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 318 | 325 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 382 | 391 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 52 | 62 | PF00244 | 0.506 |
LIG_BRCT_BRCA1_1 | 301 | 305 | PF00533 | 0.428 |
LIG_Clathr_ClatBox_1 | 230 | 234 | PF01394 | 0.470 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.514 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.591 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.500 |
LIG_LIR_Apic_2 | 329 | 335 | PF02991 | 0.563 |
LIG_LIR_Apic_2 | 348 | 352 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 96 | 104 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.455 |
LIG_MYND_1 | 45 | 49 | PF01753 | 0.472 |
LIG_PCNA_APIM_2 | 292 | 298 | PF02747 | 0.312 |
LIG_Pex14_2 | 390 | 394 | PF04695 | 0.456 |
LIG_REV1ctd_RIR_1 | 293 | 302 | PF16727 | 0.462 |
LIG_REV1ctd_RIR_1 | 388 | 394 | PF16727 | 0.464 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.653 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.461 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.455 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.442 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.748 |
LIG_SH2_NCK_1 | 289 | 293 | PF00017 | 0.461 |
LIG_SH2_PTP2 | 197 | 200 | PF00017 | 0.452 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.372 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.525 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.507 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.585 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.523 |
LIG_TRFH_1 | 349 | 353 | PF08558 | 0.575 |
LIG_TYR_ITIM | 287 | 292 | PF00017 | 0.465 |
LIG_TYR_ITIM | 82 | 87 | PF00017 | 0.539 |
MOD_CDK_SPK_2 | 75 | 80 | PF00069 | 0.438 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.720 |
MOD_CDK_SPxxK_3 | 253 | 260 | PF00069 | 0.531 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.542 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.643 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.791 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.684 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.375 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.710 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.378 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.568 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.651 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.575 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.651 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.443 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.553 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.517 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.519 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.399 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.479 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.529 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.703 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.358 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.546 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.497 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.482 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.460 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.417 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.447 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.484 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.441 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.362 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.257 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.487 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.397 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.683 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.781 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.540 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.629 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.619 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.523 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.661 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.389 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.370 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.626 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.507 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.583 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.343 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.698 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.615 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.447 |
MOD_SUMO_rev_2 | 143 | 149 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 379 | 384 | PF01217 | 0.337 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.748 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 260 | 263 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE21 | Leptomonas seymouri | 61% | 87% |
A0A0S4INY1 | Bodo saltans | 32% | 86% |
A0A1X0NGS9 | Trypanosomatidae | 36% | 100% |
A4HC41 | Leishmania braziliensis | 82% | 100% |
A4HTQ4 | Leishmania infantum | 99% | 100% |
C9ZPG1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AMJ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QI48 | Leishmania major | 93% | 100% |
V5BEE3 | Trypanosoma cruzi | 34% | 100% |