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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HJI3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.733 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.806 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.461 |
CLV_Separin_Metazoa | 43 | 47 | PF03568 | 0.684 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.819 |
DEG_SCF_FBW7_1 | 143 | 149 | PF00400 | 0.680 |
DEG_SCF_FBW7_1 | 309 | 316 | PF00400 | 0.700 |
DEG_SCF_FBW7_1 | 319 | 325 | PF00400 | 0.747 |
DEG_SPOP_SBC_1 | 313 | 317 | PF00917 | 0.857 |
DOC_CKS1_1 | 143 | 148 | PF01111 | 0.860 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.696 |
DOC_CKS1_1 | 546 | 551 | PF01111 | 0.849 |
DOC_PP2B_LxvP_1 | 490 | 493 | PF13499 | 0.685 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.673 |
DOC_PP4_FxxP_1 | 581 | 584 | PF00568 | 0.785 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.864 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.827 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.855 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.832 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.857 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.784 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.831 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.850 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.790 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 230 | 240 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 275 | 284 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 468 | 477 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 482 | 486 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 487 | 491 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 536 | 545 | PF00244 | 0.658 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.692 |
LIG_CtBP_PxDLS_1 | 71 | 75 | PF00389 | 0.669 |
LIG_deltaCOP1_diTrp_1 | 228 | 236 | PF00928 | 0.766 |
LIG_EVH1_2 | 504 | 508 | PF00568 | 0.657 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.639 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.581 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.683 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.875 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.669 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.663 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.674 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.693 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.673 |
LIG_FHA_2 | 255 | 261 | PF00498 | 0.644 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.875 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.861 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.797 |
LIG_LIR_Apic_2 | 403 | 407 | PF02991 | 0.666 |
LIG_LIR_Apic_2 | 515 | 520 | PF02991 | 0.775 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.773 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.819 |
LIG_NRBOX | 222 | 228 | PF00104 | 0.762 |
LIG_REV1ctd_RIR_1 | 362 | 372 | PF16727 | 0.849 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.826 |
LIG_SH2_GRB2like | 404 | 407 | PF00017 | 0.668 |
LIG_SH2_SRC | 404 | 407 | PF00017 | 0.668 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.662 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.672 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.693 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.835 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.669 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.684 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.707 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.849 |
LIG_SUMO_SIM_anti_2 | 598 | 604 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 496 | 503 | PF11976 | 0.761 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.674 |
LIG_WW_3 | 295 | 299 | PF00397 | 0.659 |
LIG_WW_3 | 43 | 47 | PF00397 | 0.684 |
MOD_CDK_SPK_2 | 142 | 147 | PF00069 | 0.806 |
MOD_CDK_SPK_2 | 516 | 521 | PF00069 | 0.664 |
MOD_CDK_SPK_2 | 545 | 550 | PF00069 | 0.850 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.782 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.668 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.857 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.806 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.681 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.751 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.820 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.768 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.851 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.819 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.676 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.669 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.875 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.856 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.796 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.702 |
MOD_DYRK1A_RPxSP_1 | 54 | 58 | PF00069 | 0.687 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.611 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.551 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.578 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.644 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.595 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.530 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.603 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.467 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.679 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.656 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.637 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.770 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.729 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.713 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.756 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.796 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.817 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.686 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.824 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.666 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.673 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.705 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.732 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.766 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.824 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.706 |
MOD_LATS_1 | 210 | 216 | PF00433 | 0.654 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.473 |
MOD_N-GLC_1 | 371 | 376 | PF02516 | 0.480 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.551 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.669 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.712 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.696 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.683 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.668 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.826 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.823 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.712 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.856 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.795 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.687 |
MOD_PK_1 | 190 | 196 | PF00069 | 0.662 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.660 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.791 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.685 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.692 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.686 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.764 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.669 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.702 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.813 |
MOD_Plk_2-3 | 219 | 225 | PF00069 | 0.586 |
MOD_Plk_2-3 | 245 | 251 | PF00069 | 0.673 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.659 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.823 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.715 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.778 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.857 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.834 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.767 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.807 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.784 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.686 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.831 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.809 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.651 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.687 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.850 |
MOD_SUMO_for_1 | 182 | 185 | PF00179 | 0.663 |
MOD_SUMO_rev_2 | 154 | 164 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 215 | 223 | PF00179 | 0.605 |
TRG_DiLeu_BaEn_1 | 43 | 48 | PF01217 | 0.686 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.798 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.825 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 536 | 541 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4Q2 | Leishmania donovani | 56% | 100% |
A4I732 | Leishmania infantum | 56% | 86% |
E9B200 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
Q4Q661 | Leishmania major | 54% | 98% |