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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4H835
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.768 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 258 | 260 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.556 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.501 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.465 |
DEG_SPOP_SBC_1 | 292 | 296 | PF00917 | 0.679 |
DEG_SPOP_SBC_1 | 40 | 44 | PF00917 | 0.724 |
DOC_ANK_TNKS_1 | 160 | 167 | PF00023 | 0.598 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.409 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.506 |
DOC_CYCLIN_RxL_1 | 234 | 243 | PF00134 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 18 | 24 | PF00134 | 0.780 |
DOC_MAPK_gen_1 | 332 | 340 | PF00069 | 0.656 |
DOC_MAPK_RevD_3 | 118 | 133 | PF00069 | 0.306 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.377 |
DOC_PP4_FxxP_1 | 422 | 425 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.354 |
LIG_Actin_WH2_2 | 217 | 232 | PF00022 | 0.411 |
LIG_APCC_ABBA_1 | 102 | 107 | PF00400 | 0.651 |
LIG_APCC_ABBA_1 | 208 | 213 | PF00400 | 0.648 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.764 |
LIG_BRCT_BRCA1_1 | 102 | 106 | PF00533 | 0.439 |
LIG_BRCT_BRCA1_1 | 360 | 364 | PF00533 | 0.439 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.741 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.475 |
LIG_LIR_Apic_2 | 146 | 151 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 103 | 114 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 196 | 203 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 222 | 231 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 23 | 28 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 268 | 278 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.446 |
LIG_Pex14_2 | 102 | 106 | PF04695 | 0.439 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.397 |
LIG_Pex14_2 | 144 | 148 | PF04695 | 0.219 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 355 | 359 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.446 |
LIG_SH3_1 | 351 | 357 | PF00018 | 0.579 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.418 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.480 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.291 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.419 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.686 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.773 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.643 |
LIG_TRAF2_1 | 365 | 368 | PF00917 | 0.476 |
LIG_TRFH_1 | 199 | 203 | PF08558 | 0.665 |
LIG_TRFH_1 | 270 | 274 | PF08558 | 0.474 |
LIG_UBA3_1 | 443 | 450 | PF00899 | 0.582 |
LIG_WRC_WIRS_1 | 145 | 150 | PF05994 | 0.397 |
MOD_CDK_SPK_2 | 149 | 154 | PF00069 | 0.404 |
MOD_CDK_SPxxK_3 | 353 | 360 | PF00069 | 0.503 |
MOD_CDK_SPxxK_3 | 41 | 48 | PF00069 | 0.432 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.793 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.639 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.631 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.581 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.458 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.578 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.443 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.343 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.376 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.659 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.638 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.733 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.529 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.401 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.754 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.670 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.770 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.693 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.683 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.638 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.435 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.508 |
MOD_N-GLC_1 | 193 | 198 | PF02516 | 0.649 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.425 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.669 |
MOD_N-GLC_2 | 347 | 349 | PF02516 | 0.348 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.442 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.692 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.534 |
MOD_NEK2_2 | 100 | 105 | PF00069 | 0.464 |
MOD_NEK2_2 | 445 | 450 | PF00069 | 0.589 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.551 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.532 |
MOD_PK_1 | 48 | 54 | PF00069 | 0.311 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.774 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.707 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.634 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.552 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.525 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.386 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.730 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.512 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.484 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.650 |
MOD_SUMO_rev_2 | 238 | 246 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 325 | 335 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 80 | 86 | PF00179 | 0.589 |
TRG_DiLeu_BaEn_1 | 380 | 385 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_4 | 213 | 219 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 116 | 121 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 408 | 413 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 355 | 358 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 351 | 353 | PF00400 | 0.569 |
TRG_NES_CRM1_1 | 216 | 227 | PF08389 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I615 | Leptomonas seymouri | 72% | 100% |
A0A1X0NTS1 | Trypanosomatidae | 39% | 100% |
A0A3S5H6U7 | Leishmania donovani | 76% | 100% |
A0A422NLQ5 | Trypanosoma rangeli | 39% | 100% |
A4HWG0 | Leishmania infantum | 76% | 100% |
C9ZP02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AQ60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QFC3 | Leishmania major | 78% | 99% |