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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4QDZ0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.811 |
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.773 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.763 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.809 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.521 |
CLV_PCSK_FUR_1 | 170 | 174 | PF00082 | 0.640 |
CLV_PCSK_FUR_1 | 372 | 376 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.798 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.869 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.772 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.523 |
CLV_Separin_Metazoa | 492 | 496 | PF03568 | 0.662 |
DEG_APCC_DBOX_1 | 483 | 491 | PF00400 | 0.691 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.546 |
DEG_SPOP_SBC_1 | 165 | 169 | PF00917 | 0.800 |
DEG_SPOP_SBC_1 | 205 | 209 | PF00917 | 0.794 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.756 |
DEG_SPOP_SBC_1 | 407 | 411 | PF00917 | 0.597 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.667 |
DOC_CKS1_1 | 415 | 420 | PF01111 | 0.615 |
DOC_CYCLIN_yCln2_LP_2 | 251 | 257 | PF00134 | 0.751 |
DOC_CYCLIN_yCln2_LP_2 | 536 | 542 | PF00134 | 0.817 |
DOC_MAPK_gen_1 | 513 | 521 | PF00069 | 0.599 |
DOC_MAPK_gen_1 | 601 | 610 | PF00069 | 0.518 |
DOC_PP2B_LxvP_1 | 536 | 539 | PF13499 | 0.820 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.801 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.765 |
DOC_USP7_MATH_2 | 547 | 553 | PF00917 | 0.642 |
DOC_USP7_UBL2_3 | 172 | 176 | PF12436 | 0.804 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.849 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 110 | 116 | PF00244 | 0.803 |
LIG_14-3-3_CanoR_1 | 199 | 205 | PF00244 | 0.770 |
LIG_14-3-3_CanoR_1 | 346 | 353 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 464 | 472 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 601 | 611 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 450 | 468 | PF00022 | 0.670 |
LIG_Actin_WH2_2 | 490 | 507 | PF00022 | 0.596 |
LIG_APCC_ABBA_1 | 263 | 268 | PF00400 | 0.795 |
LIG_CaM_IQ_9 | 497 | 512 | PF13499 | 0.653 |
LIG_eIF4E_1 | 250 | 256 | PF01652 | 0.757 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.682 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.680 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.516 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.628 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.708 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.675 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.582 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.758 |
LIG_LIR_Apic_2 | 91 | 96 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.575 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.832 |
LIG_SH2_SRC | 250 | 253 | PF00017 | 0.768 |
LIG_SH2_STAP1 | 586 | 590 | PF00017 | 0.633 |
LIG_SH2_STAT3 | 611 | 614 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.830 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.521 |
LIG_SH3_2 | 223 | 228 | PF14604 | 0.840 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.783 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.684 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.817 |
LIG_TRAF2_1 | 286 | 289 | PF00917 | 0.831 |
LIG_TRAF2_1 | 547 | 550 | PF00917 | 0.711 |
LIG_UBA3_1 | 232 | 236 | PF00899 | 0.805 |
MOD_CDK_SPK_2 | 179 | 184 | PF00069 | 0.811 |
MOD_CDK_SPK_2 | 194 | 199 | PF00069 | 0.665 |
MOD_CDK_SPK_2 | 60 | 65 | PF00069 | 0.756 |
MOD_CDK_SPxxK_3 | 179 | 186 | PF00069 | 0.836 |
MOD_CDK_SPxxK_3 | 187 | 194 | PF00069 | 0.750 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.868 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.560 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.682 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.858 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.747 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.626 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.629 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.752 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.771 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.779 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.706 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.585 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.765 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.599 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.616 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.660 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.541 |
MOD_Cter_Amidation | 117 | 120 | PF01082 | 0.772 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.835 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.766 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.842 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.626 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.768 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.765 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.798 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.705 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.616 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.852 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.808 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.652 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.722 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.562 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.788 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.694 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.563 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.851 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.666 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.736 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.646 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.520 |
MOD_LATS_1 | 161 | 167 | PF00433 | 0.833 |
MOD_LATS_1 | 335 | 341 | PF00433 | 0.566 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.795 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.605 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.602 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.622 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.809 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.498 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.667 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.862 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.862 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.791 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.682 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.644 |
MOD_PIKK_1 | 610 | 616 | PF00454 | 0.670 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.642 |
MOD_PKA_1 | 44 | 50 | PF00069 | 0.730 |
MOD_PKA_1 | 601 | 607 | PF00069 | 0.678 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.655 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.615 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.730 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.706 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.656 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.678 |
MOD_PKB_1 | 462 | 470 | PF00069 | 0.676 |
MOD_Plk_1 | 549 | 555 | PF00069 | 0.631 |
MOD_Plk_1 | 577 | 583 | PF00069 | 0.665 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.672 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.794 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.739 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.635 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.628 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.569 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.850 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.757 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.664 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.739 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.807 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.609 |
MOD_SUMO_for_1 | 138 | 141 | PF00179 | 0.754 |
MOD_SUMO_for_1 | 394 | 397 | PF00179 | 0.688 |
MOD_SUMO_rev_2 | 168 | 178 | PF00179 | 0.791 |
TRG_DiLeu_BaEn_4 | 288 | 294 | PF01217 | 0.596 |
TRG_DiLeu_BaEn_4 | 387 | 393 | PF01217 | 0.667 |
TRG_DiLeu_BaEn_4 | 516 | 522 | PF01217 | 0.663 |
TRG_DiLeu_BaEn_4 | 549 | 555 | PF01217 | 0.693 |
TRG_DiLeu_BaLyEn_6 | 93 | 98 | PF01217 | 0.606 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 44 | 46 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 581 | 584 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 601 | 603 | PF00400 | 0.355 |
TRG_NLS_MonoExtN_4 | 372 | 377 | PF00514 | 0.667 |
TRG_Pf-PMV_PEXEL_1 | 556 | 560 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 595 | 600 | PF00026 | 0.594 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IAX8 | Leishmania donovani | 89% | 85% |
A4H9G0 | Leishmania braziliensis | 68% | 100% |
A4HXS7 | Leishmania infantum | 89% | 85% |
E9ARI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 85% |