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: Q4QFC3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.747 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 116 | 124 | PF00400 | 0.499 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.464 |
DOC_ANK_TNKS_1 | 162 | 169 | PF00023 | 0.594 |
DOC_CKS1_1 | 152 | 157 | PF01111 | 0.403 |
DOC_CKS1_1 | 351 | 356 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 236 | 245 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 18 | 24 | PF00134 | 0.787 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 329 | 337 | PF00069 | 0.659 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.546 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.372 |
DOC_PP4_FxxP_1 | 419 | 422 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 58 | 61 | PF00568 | 0.291 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.793 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.687 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.695 |
LIG_14-3-3_CanoR_1 | 221 | 226 | PF00244 | 0.462 |
LIG_14-3-3_CterR_2 | 444 | 448 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 219 | 234 | PF00022 | 0.402 |
LIG_APCC_ABBA_1 | 210 | 215 | PF00400 | 0.618 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.772 |
LIG_BIR_III_2 | 109 | 113 | PF00653 | 0.489 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.541 |
LIG_BRCT_BRCA1_1 | 357 | 361 | PF00533 | 0.466 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.746 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.457 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.636 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.484 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.703 |
LIG_LIR_Apic_2 | 148 | 153 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 198 | 205 | PF02991 | 0.630 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.468 |
LIG_MYND_1 | 9 | 13 | PF01753 | 0.556 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.391 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.211 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.668 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.446 |
LIG_SH3_1 | 348 | 354 | PF00018 | 0.578 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.412 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.613 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.478 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.689 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.418 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.728 |
LIG_SUMO_SIM_par_1 | 439 | 445 | PF11976 | 0.519 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.778 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.657 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.481 |
LIG_TRFH_1 | 201 | 205 | PF08558 | 0.661 |
LIG_UBA3_1 | 360 | 366 | PF00899 | 0.517 |
LIG_UBA3_1 | 440 | 447 | PF00899 | 0.578 |
LIG_WRC_WIRS_1 | 147 | 152 | PF05994 | 0.391 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 350 | 357 | PF00069 | 0.499 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.573 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.788 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.484 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.337 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.775 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.812 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.501 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.572 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.684 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.683 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.448 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.637 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.723 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.521 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.642 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.393 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.768 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.757 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.635 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.739 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.677 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.585 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.632 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.440 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.638 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.635 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.666 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.659 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.635 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.430 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.704 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.743 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.413 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.701 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.558 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.616 |
MOD_NEK2_2 | 442 | 447 | PF00069 | 0.584 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.552 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.637 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.719 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.660 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.643 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.547 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.438 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.547 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.381 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.561 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.726 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.477 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 322 | 332 | PF00179 | 0.603 |
MOD_SUMO_rev_2 | 358 | 367 | PF00179 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 405 | 410 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.571 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.570 |
TRG_NES_CRM1_1 | 218 | 229 | PF08389 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I615 | Leptomonas seymouri | 71% | 100% |
A0A1X0NTS1 | Trypanosomatidae | 37% | 100% |
A0A3S5H6U7 | Leishmania donovani | 93% | 100% |
A0A422NLQ5 | Trypanosoma rangeli | 37% | 100% |
A4H835 | Leishmania braziliensis | 78% | 99% |
A4HWG0 | Leishmania infantum | 93% | 100% |
C9ZP02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AQ60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |