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: A4HMA4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.655 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.443 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.534 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 438 | 442 | PF00917 | 0.511 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.483 |
DOC_CYCLIN_RxL_1 | 89 | 98 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 303 | PF00134 | 0.451 |
DOC_MAPK_FxFP_2 | 355 | 358 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 120 | 128 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.586 |
DOC_MAPK_MEF2A_6 | 164 | 172 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 182 | 191 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 1 | 7 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 456 | 462 | PF00149 | 0.591 |
DOC_PP1_RVXF_1 | 90 | 97 | PF00149 | 0.565 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.599 |
DOC_PP4_FxxP_1 | 355 | 358 | PF00568 | 0.512 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.686 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 217 | 222 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 30 | 36 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 471 | 477 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 482 | 487 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 56 | 61 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 68 | 72 | PF00244 | 0.385 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.563 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.580 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.753 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.536 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.657 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.605 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.776 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.621 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.734 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.323 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.518 |
LIG_GBD_Chelix_1 | 187 | 195 | PF00786 | 0.339 |
LIG_LIR_Apic_2 | 352 | 358 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 20 | 29 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 220 | 228 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 406 | 417 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 5 | 9 | PF02991 | 0.591 |
LIG_LYPXL_yS_3 | 357 | 360 | PF13949 | 0.755 |
LIG_PDZ_Class_1 | 506 | 511 | PF00595 | 0.687 |
LIG_Pex14_1 | 15 | 19 | PF04695 | 0.470 |
LIG_Pex14_1 | 301 | 305 | PF04695 | 0.456 |
LIG_Pex14_1 | 461 | 465 | PF04695 | 0.632 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.406 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.673 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.462 |
LIG_SH2_GRB2like | 87 | 90 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 409 | 413 | PF00017 | 0.673 |
LIG_SH2_NCK_1 | 489 | 493 | PF00017 | 0.725 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.383 |
LIG_SH2_PTP2 | 223 | 226 | PF00017 | 0.639 |
LIG_SH2_PTP2 | 376 | 379 | PF00017 | 0.659 |
LIG_SH2_SRC | 320 | 323 | PF00017 | 0.717 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 316 | 320 | PF00017 | 0.634 |
LIG_SH2_STAP1 | 489 | 493 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.449 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.517 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.613 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.713 |
LIG_SUMO_SIM_par_1 | 199 | 208 | PF11976 | 0.680 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.466 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.702 |
LIG_TYR_ITSM | 217 | 224 | PF00017 | 0.430 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.704 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.714 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.696 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.532 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.583 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.675 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.663 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.661 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.323 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.565 |
MOD_DYRK1A_RPxSP_1 | 164 | 168 | PF00069 | 0.602 |
MOD_DYRK1A_RPxSP_1 | 68 | 72 | PF00069 | 0.432 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.700 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.432 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.652 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.681 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.511 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.700 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.674 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.682 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.615 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.437 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.665 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.666 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.358 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.611 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.625 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.672 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.771 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.535 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.519 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.636 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.628 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.398 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.630 |
MOD_N-GLC_1 | 226 | 231 | PF02516 | 0.572 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.504 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.566 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.540 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.627 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.706 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.435 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.434 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.490 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.590 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.344 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.682 |
MOD_PK_1 | 247 | 253 | PF00069 | 0.488 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.469 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.686 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.381 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.638 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.681 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.607 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.538 |
MOD_PKB_1 | 247 | 255 | PF00069 | 0.494 |
MOD_PKB_1 | 403 | 411 | PF00069 | 0.742 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.622 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.717 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.740 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.593 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.546 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.553 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.391 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.469 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.738 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.469 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.390 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.607 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.594 |
MOD_SUMO_rev_2 | 193 | 200 | PF00179 | 0.657 |
TRG_DiLeu_BaEn_1 | 196 | 201 | PF01217 | 0.652 |
TRG_DiLeu_BaEn_1 | 343 | 348 | PF01217 | 0.740 |
TRG_DiLeu_BaLyEn_6 | 165 | 170 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 241 | 246 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.659 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.693 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.652 |
TRG_NES_CRM1_1 | 118 | 130 | PF08389 | 0.587 |
TRG_NES_CRM1_1 | 190 | 205 | PF08389 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.703 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5S8 | Leptomonas seymouri | 40% | 99% |
A0A0S4JCU2 | Bodo saltans | 22% | 100% |
A0A3S7X8U0 | Leishmania donovani | 74% | 100% |
A4IAW9 | Leishmania infantum | 74% | 100% |
E9AEP7 | Leishmania major | 73% | 100% |
E9B5V2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
V5DJL7 | Trypanosoma cruzi | 27% | 100% |