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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q2C7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 443 | 447 | PF00656 | 0.730 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.608 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.534 |
CLV_Separin_Metazoa | 110 | 114 | PF03568 | 0.684 |
CLV_Separin_Metazoa | 44 | 48 | PF03568 | 0.664 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.666 |
DEG_COP1_1 | 425 | 433 | PF00400 | 0.585 |
DOC_CYCLIN_RxL_1 | 33 | 44 | PF00134 | 0.553 |
DOC_MAPK_gen_1 | 104 | 114 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 33 | 42 | PF00069 | 0.671 |
DOC_PP1_RVXF_1 | 336 | 342 | PF00149 | 0.704 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.610 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.636 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.691 |
DOC_USP7_MATH_2 | 175 | 181 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.772 |
DOC_USP7_UBL2_3 | 78 | 82 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.784 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 370 | 380 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 405 | 415 | PF00244 | 0.797 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.638 |
LIG_Actin_WH2_2 | 190 | 207 | PF00022 | 0.554 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.807 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.693 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.639 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.697 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.754 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.681 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.797 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.677 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.605 |
LIG_LIR_Apic_2 | 446 | 451 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.625 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.795 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.657 |
LIG_PTAP_UEV_1 | 383 | 388 | PF05743 | 0.794 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.717 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.666 |
LIG_SH2_GRB2like | 117 | 120 | PF00017 | 0.562 |
LIG_SH2_NCK_1 | 276 | 280 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.660 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.713 |
LIG_SH3_1 | 141 | 147 | PF00018 | 0.690 |
LIG_SH3_2 | 236 | 241 | PF14604 | 0.605 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.672 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.766 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.798 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.733 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.638 |
LIG_SH3_5 | 414 | 418 | PF00018 | 0.703 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.751 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.751 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.673 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.476 |
LIG_UBA3_1 | 203 | 212 | PF00899 | 0.578 |
LIG_WW_3 | 413 | 417 | PF00397 | 0.816 |
MOD_CDC14_SPxK_1 | 157 | 160 | PF00782 | 0.727 |
MOD_CDC14_SPxK_1 | 286 | 289 | PF00782 | 0.658 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.741 |
MOD_CDK_SPK_2 | 289 | 294 | PF00069 | 0.663 |
MOD_CDK_SPxK_1 | 154 | 160 | PF00069 | 0.732 |
MOD_CDK_SPxK_1 | 283 | 289 | PF00069 | 0.661 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.743 |
MOD_CDK_SPxxK_3 | 154 | 161 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.745 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.581 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.717 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.697 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.724 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.710 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.679 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.597 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.753 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.608 |
MOD_Cter_Amidation | 368 | 371 | PF01082 | 0.678 |
MOD_DYRK1A_RPxSP_1 | 308 | 312 | PF00069 | 0.690 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.679 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.646 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.684 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.579 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.783 |
MOD_GlcNHglycan | 360 | 364 | PF01048 | 0.523 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.642 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.737 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.684 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.705 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.656 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.587 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.670 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.755 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.677 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.703 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.661 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.709 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.677 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.669 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.688 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.757 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.602 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.794 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.677 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.665 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.678 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.589 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.756 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.689 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.663 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.664 |
MOD_Plk_2-3 | 31 | 37 | PF00069 | 0.674 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.718 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.779 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.679 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.648 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.707 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.725 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.672 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.538 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.697 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.711 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.782 |
MOD_SUMO_for_1 | 455 | 458 | PF00179 | 0.733 |
MOD_SUMO_rev_2 | 208 | 215 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.756 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.692 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 268 | 273 | PF00026 | 0.785 |
TRG_Pf-PMV_PEXEL_1 | 38 | 43 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P706 | Leptomonas seymouri | 33% | 89% |
A0A3S7X8Q0 | Leishmania donovani | 85% | 100% |
A4HBD7 | Leishmania braziliensis | 58% | 99% |
A4IAI5 | Leishmania infantum | 85% | 100% |
E9B5K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |