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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HQJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 6 | 10 | PF00656 | 0.548 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.764 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.421 |
CLV_PCSK_FUR_1 | 83 | 87 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.432 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.643 |
DEG_SCF_FBW7_1 | 443 | 449 | PF00400 | 0.635 |
DEG_SCF_TRCP1_1 | 306 | 312 | PF00400 | 0.379 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.483 |
DOC_CDC14_PxL_1 | 253 | 261 | PF14671 | 0.537 |
DOC_CKS1_1 | 415 | 420 | PF01111 | 0.660 |
DOC_CKS1_1 | 443 | 448 | PF01111 | 0.629 |
DOC_CYCLIN_RxL_1 | 398 | 410 | PF00134 | 0.624 |
DOC_CYCLIN_RxL_1 | 466 | 477 | PF00134 | 0.599 |
DOC_MAPK_DCC_7 | 251 | 261 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 143 | 150 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 401 | 408 | PF00149 | 0.615 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.598 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.628 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 145 | 149 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 341 | 351 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 451 | 456 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 64 | 73 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 84 | 90 | PF00244 | 0.613 |
LIG_Actin_WH2_2 | 146 | 161 | PF00022 | 0.562 |
LIG_Actin_WH2_2 | 30 | 48 | PF00022 | 0.475 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.565 |
LIG_eIF4E_1 | 73 | 79 | PF01652 | 0.490 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.567 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.618 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.543 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.668 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.580 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.521 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.570 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.603 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.615 |
LIG_GBD_Chelix_1 | 467 | 475 | PF00786 | 0.396 |
LIG_LIR_Gen_1 | 135 | 142 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 474 | 481 | PF02991 | 0.665 |
LIG_LIR_LC3C_4 | 112 | 117 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.656 |
LIG_PDZ_Class_2 | 476 | 481 | PF00595 | 0.577 |
LIG_Pex14_1 | 133 | 137 | PF04695 | 0.632 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.549 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.448 |
LIG_Rb_pABgroove_1 | 403 | 411 | PF01858 | 0.600 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.641 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.537 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.413 |
LIG_SH2_PTP2 | 18 | 21 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.538 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.579 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.223 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.338 |
LIG_SH3_CIN85_PxpxPR_1 | 267 | 272 | PF14604 | 0.466 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 257 | 262 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 30 | 35 | PF11976 | 0.642 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.669 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.687 |
LIG_TRFH_1 | 476 | 480 | PF08558 | 0.568 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.413 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.595 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.535 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.563 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.676 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.673 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.594 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.559 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.638 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.573 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.315 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.316 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.423 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.679 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.726 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.708 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.280 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.428 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.357 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.457 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.482 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.608 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.741 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.552 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.614 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.450 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.567 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.463 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.673 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.591 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.577 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.654 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.567 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.582 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.388 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.578 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.656 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.637 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.608 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.607 |
MOD_PIKK_1 | 446 | 452 | PF00454 | 0.646 |
MOD_PKA_1 | 85 | 91 | PF00069 | 0.606 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.548 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.613 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.562 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.606 |
MOD_PKB_1 | 83 | 91 | PF00069 | 0.682 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.539 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.709 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.624 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.559 |
MOD_Plk_2-3 | 194 | 200 | PF00069 | 0.583 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.634 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.561 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.561 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.477 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.653 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.588 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.579 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.661 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.632 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.649 |
TRG_DiLeu_BaEn_1 | 200 | 205 | PF01217 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.611 |
TRG_DiLeu_BaLyEn_6 | 243 | 248 | PF01217 | 0.576 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.292 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.621 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 402 | 404 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 83 | 86 | PF00400 | 0.632 |
TRG_NES_CRM1_1 | 128 | 144 | PF08389 | 0.535 |
TRG_NLS_MonoExtN_4 | 360 | 365 | PF00514 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 190 | 194 | PF00026 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.338 |
TRG_Pf-PMV_PEXEL_1 | 85 | 90 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDR4 | Leptomonas seymouri | 64% | 100% |
A0A0S4ISX7 | Bodo saltans | 27% | 100% |
A0A1X0NN06 | Trypanosomatidae | 43% | 100% |
A0A3Q8IM62 | Leishmania donovani | 81% | 100% |
A0A3R7MQC3 | Trypanosoma rangeli | 43% | 100% |
D0A3P1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AI02 | Leishmania infantum | 81% | 100% |
E9AUA6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q085 | Leishmania major | 80% | 98% |
V5BHM6 | Trypanosoma cruzi | 41% | 100% |