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: A0A3S7X8Q0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 324 | 328 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.591 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 38 | 40 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.606 |
CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.621 |
CLV_PCSK_FUR_1 | 36 | 40 | PF00082 | 0.569 |
CLV_PCSK_FUR_1 | 50 | 54 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.529 |
CLV_Separin_Metazoa | 110 | 114 | PF03568 | 0.681 |
CLV_Separin_Metazoa | 44 | 48 | PF03568 | 0.653 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.660 |
DEG_SPOP_SBC_1 | 243 | 247 | PF00917 | 0.632 |
DOC_ANK_TNKS_1 | 420 | 427 | PF00023 | 0.621 |
DOC_CYCLIN_RxL_1 | 150 | 159 | PF00134 | 0.645 |
DOC_CYCLIN_RxL_1 | 33 | 44 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 236 | 242 | PF00134 | 0.585 |
DOC_MAPK_gen_1 | 104 | 114 | PF00069 | 0.639 |
DOC_MAPK_gen_1 | 33 | 42 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 335 | 342 | PF00149 | 0.731 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.635 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.681 |
DOC_PP4_FxxP_1 | 448 | 451 | PF00568 | 0.697 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.783 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.714 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.813 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.784 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 232 | 240 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 274 | 283 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 370 | 374 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.785 |
LIG_14-3-3_CanoR_1 | 90 | 96 | PF00244 | 0.644 |
LIG_Actin_WH2_2 | 190 | 207 | PF00022 | 0.538 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.783 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.631 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.722 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.752 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.786 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.811 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.709 |
LIG_Integrin_isoDGR_2 | 349 | 351 | PF01839 | 0.591 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.805 |
LIG_LIR_Nem_3 | 458 | 464 | PF02991 | 0.752 |
LIG_PTAP_UEV_1 | 383 | 388 | PF05743 | 0.806 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.725 |
LIG_SH2_CRK | 376 | 380 | PF00017 | 0.670 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.786 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.734 |
LIG_SH3_1 | 141 | 147 | PF00018 | 0.699 |
LIG_SH3_2 | 411 | 416 | PF14604 | 0.646 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.682 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.823 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.748 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.625 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.688 |
LIG_SH3_5 | 414 | 418 | PF00018 | 0.707 |
LIG_SH3_CIN85_PxpxPR_1 | 411 | 416 | PF14604 | 0.568 |
LIG_SUMO_SIM_anti_2 | 177 | 183 | PF11976 | 0.691 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.635 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.671 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.470 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.493 |
LIG_WW_3 | 413 | 417 | PF00397 | 0.817 |
LIG_WW_3 | 75 | 79 | PF00397 | 0.613 |
MOD_CDC14_SPxK_1 | 286 | 289 | PF00782 | 0.667 |
MOD_CDC14_SPxK_1 | 292 | 295 | PF00782 | 0.679 |
MOD_CDC14_SPxK_1 | 301 | 304 | PF00782 | 0.757 |
MOD_CDK_SPK_2 | 289 | 294 | PF00069 | 0.683 |
MOD_CDK_SPxK_1 | 283 | 289 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.761 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.748 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.704 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.813 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.649 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.714 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.672 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.590 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.770 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.780 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.716 |
MOD_Cter_Amidation | 368 | 371 | PF01082 | 0.683 |
MOD_DYRK1A_RPxSP_1 | 142 | 146 | PF00069 | 0.604 |
MOD_DYRK1A_RPxSP_1 | 308 | 312 | PF00069 | 0.695 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.658 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.672 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.619 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.683 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.753 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.576 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.604 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.805 |
MOD_GlcNHglycan | 360 | 364 | PF01048 | 0.531 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.681 |
MOD_GlcNHglycan | 417 | 421 | PF01048 | 0.717 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.786 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.723 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.666 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.672 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.684 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.698 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.643 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.739 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.714 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.802 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.644 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.705 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.635 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.695 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.671 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.727 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.796 |
MOD_PIKK_1 | 166 | 172 | PF00454 | 0.647 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.737 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.555 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.786 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.671 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.686 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.694 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.594 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.700 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.671 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.659 |
MOD_Plk_2-3 | 177 | 183 | PF00069 | 0.657 |
MOD_Plk_2-3 | 31 | 37 | PF00069 | 0.668 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.725 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.723 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.703 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.665 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.714 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.691 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.744 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.812 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.731 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.784 |
MOD_SUMO_for_1 | 455 | 458 | PF00179 | 0.750 |
MOD_SUMO_rev_2 | 208 | 215 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 30 | 35 | PF00179 | 0.632 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.755 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.693 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.624 |
TRG_Pf-PMV_PEXEL_1 | 268 | 273 | PF00026 | 0.784 |
TRG_Pf-PMV_PEXEL_1 | 38 | 43 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P706 | Leptomonas seymouri | 35% | 89% |
A4HBD7 | Leishmania braziliensis | 57% | 100% |
A4IAI5 | Leishmania infantum | 99% | 100% |
E9B5K9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q2C7 | Leishmania major | 85% | 100% |