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: A4IB03
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 289 | 293 | PF00656 | 0.846 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.836 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.847 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.844 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.833 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.816 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.811 |
CLV_PCSK_FUR_1 | 114 | 118 | PF00082 | 0.680 |
CLV_PCSK_FUR_1 | 137 | 141 | PF00082 | 0.749 |
CLV_PCSK_FUR_1 | 19 | 23 | PF00082 | 0.639 |
CLV_PCSK_FUR_1 | 306 | 310 | PF00082 | 0.790 |
CLV_PCSK_FUR_1 | 38 | 42 | PF00082 | 0.654 |
CLV_PCSK_FUR_1 | 391 | 395 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.833 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.805 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.831 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.811 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.846 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.787 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.673 |
CLV_PCSK_PC7_1 | 140 | 146 | PF00082 | 0.831 |
CLV_PCSK_PC7_1 | 17 | 23 | PF00082 | 0.759 |
CLV_PCSK_PC7_1 | 38 | 44 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.772 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.756 |
DEG_APCC_DBOX_1 | 359 | 367 | PF00400 | 0.621 |
DEG_APCC_KENBOX_2 | 509 | 513 | PF00400 | 0.747 |
DEG_SPOP_SBC_1 | 204 | 208 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 430 | 434 | PF00917 | 0.713 |
DOC_ANK_TNKS_1 | 67 | 74 | PF00023 | 0.702 |
DOC_CKS1_1 | 529 | 534 | PF01111 | 0.813 |
DOC_CYCLIN_RxL_1 | 235 | 244 | PF00134 | 0.773 |
DOC_MAPK_gen_1 | 236 | 242 | PF00069 | 0.566 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.773 |
DOC_PP4_FxxP_1 | 534 | 537 | PF00568 | 0.712 |
DOC_PP4_MxPP_1 | 270 | 273 | PF00568 | 0.797 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.623 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 125 | 133 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 309 | 315 | PF00244 | 0.840 |
LIG_14-3-3_CanoR_1 | 85 | 95 | PF00244 | 0.843 |
LIG_14-3-3_CterR_2 | 575 | 580 | PF00244 | 0.640 |
LIG_BIR_III_2 | 519 | 523 | PF00653 | 0.644 |
LIG_BIR_III_4 | 247 | 251 | PF00653 | 0.803 |
LIG_BIR_III_4 | 474 | 478 | PF00653 | 0.726 |
LIG_EVH1_1 | 523 | 527 | PF00568 | 0.773 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.674 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.475 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.710 |
LIG_Integrin_isoDGR_2 | 572 | 574 | PF01839 | 0.681 |
LIG_LIR_Apic_2 | 335 | 341 | PF02991 | 0.787 |
LIG_LIR_Apic_2 | 531 | 537 | PF02991 | 0.710 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.831 |
LIG_MAD2 | 85 | 93 | PF02301 | 0.784 |
LIG_PTB_Apo_2 | 564 | 571 | PF02174 | 0.648 |
LIG_PTB_Phospho_1 | 564 | 570 | PF10480 | 0.652 |
LIG_RPA_C_Fungi | 241 | 253 | PF08784 | 0.543 |
LIG_SH2_GRB2like | 570 | 573 | PF00017 | 0.673 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.773 |
LIG_SH2_NCK_1 | 406 | 410 | PF00017 | 0.559 |
LIG_SH2_SRC | 535 | 538 | PF00017 | 0.767 |
LIG_SH2_SRC | 570 | 573 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.808 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.673 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.664 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.656 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.681 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 452 | 460 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 452 | 460 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 547 | 552 | PF11976 | 0.635 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.829 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.770 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.805 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.636 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.745 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.741 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.642 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.766 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.748 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.711 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.660 |
MOD_Cter_Amidation | 1 | 4 | PF01082 | 0.754 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.811 |
MOD_Cter_Amidation | 142 | 145 | PF01082 | 0.754 |
MOD_Cter_Amidation | 161 | 164 | PF01082 | 0.527 |
MOD_Cter_Amidation | 572 | 575 | PF01082 | 0.680 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.715 |
MOD_GlcNHglycan | 247 | 251 | PF01048 | 0.803 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.774 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.687 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.675 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.778 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.832 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.861 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.849 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.793 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.668 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.730 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.603 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.754 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.790 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.542 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.832 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.680 |
MOD_LATS_1 | 57 | 63 | PF00433 | 0.758 |
MOD_LATS_1 | 65 | 71 | PF00433 | 0.667 |
MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.617 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.776 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.619 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.822 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.753 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.797 |
MOD_N-GLC_2 | 423 | 425 | PF02516 | 0.611 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.667 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.722 |
MOD_PKA_1 | 43 | 49 | PF00069 | 0.728 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.743 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.787 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.766 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.778 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.820 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.831 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.523 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.730 |
MOD_PKB_1 | 123 | 131 | PF00069 | 0.679 |
MOD_PKB_1 | 41 | 49 | PF00069 | 0.731 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.755 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.777 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.826 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.652 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.800 |
MOD_Plk_2-3 | 45 | 51 | PF00069 | 0.816 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.615 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.802 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.598 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.752 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.611 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.817 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.680 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.824 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.790 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.812 |
TRG_ER_diArg_1 | 19 | 22 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 220 | 223 | PF00400 | 0.789 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.823 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.767 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.826 |
TRG_ER_diArg_1 | 38 | 41 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.731 |
TRG_ER_diArg_1 | 574 | 576 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.828 |
TRG_NLS_Bipartite_1 | 220 | 240 | PF00514 | 0.589 |
TRG_NLS_MonoExtC_3 | 162 | 167 | PF00514 | 0.789 |
TRG_Pf-PMV_PEXEL_1 | 227 | 232 | PF00026 | 0.614 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X8W4 | Leishmania donovani | 99% | 100% |
A4HFF4 | Leishmania braziliensis | 66% | 100% |
E9AET1 | Leishmania major | 87% | 100% |
E9B5Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |