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: Q4QH46
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.756 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.743 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.640 |
DEG_SIAH_1 | 472 | 480 | PF03145 | 0.692 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.754 |
DOC_CKS1_1 | 130 | 135 | PF01111 | 0.736 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.698 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.592 |
DOC_USP7_MATH_2 | 96 | 102 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.777 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 326 | 334 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.656 |
LIG_Actin_WH2_2 | 191 | 207 | PF00022 | 0.687 |
LIG_Actin_WH2_2 | 306 | 323 | PF00022 | 0.737 |
LIG_BIR_III_2 | 435 | 439 | PF00653 | 0.618 |
LIG_BIR_III_4 | 251 | 255 | PF00653 | 0.654 |
LIG_Clathr_ClatBox_1 | 264 | 268 | PF01394 | 0.786 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.752 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.757 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.744 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.622 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.654 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.643 |
LIG_GBD_Chelix_1 | 180 | 188 | PF00786 | 0.683 |
LIG_HP1_1 | 479 | 483 | PF01393 | 0.749 |
LIG_LIR_Apic_2 | 297 | 303 | PF02991 | 0.743 |
LIG_LIR_Apic_2 | 442 | 447 | PF02991 | 0.668 |
LIG_LIR_Gen_1 | 308 | 316 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 349 | 358 | PF02991 | 0.698 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.730 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.746 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.689 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.753 |
LIG_SH2_CRK | 444 | 448 | PF00017 | 0.700 |
LIG_SH2_NCK_1 | 127 | 131 | PF00017 | 0.753 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.739 |
LIG_SH3_1 | 127 | 133 | PF00018 | 0.748 |
LIG_SH3_1 | 371 | 377 | PF00018 | 0.611 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.799 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.706 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.692 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.643 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.600 |
LIG_SH3_4 | 103 | 110 | PF00018 | 0.614 |
LIG_SUMO_SIM_anti_2 | 308 | 315 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 478 | 484 | PF11976 | 0.655 |
LIG_SUMO_SIM_par_1 | 262 | 268 | PF11976 | 0.717 |
LIG_TRFH_1 | 257 | 261 | PF08558 | 0.678 |
LIG_TRFH_1 | 299 | 303 | PF08558 | 0.706 |
LIG_UBA3_1 | 301 | 307 | PF00899 | 0.496 |
LIG_WW_3 | 323 | 327 | PF00397 | 0.697 |
MOD_CDK_SPK_2 | 396 | 401 | PF00069 | 0.808 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.602 |
MOD_CDK_SPxxK_3 | 12 | 19 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 352 | 359 | PF00069 | 0.680 |
MOD_CDK_SPxxK_3 | 394 | 401 | PF00069 | 0.747 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.774 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.487 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.716 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.505 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.721 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.717 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.789 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.567 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.703 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.565 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.591 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.757 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.633 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.684 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.817 |
MOD_GlcNHglycan | 121 | 125 | PF01048 | 0.660 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.566 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.609 |
MOD_GlcNHglycan | 171 | 176 | PF01048 | 0.594 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.641 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.706 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.688 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.749 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.621 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.760 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.745 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.596 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.693 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.591 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.752 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.578 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.667 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.747 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.816 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.556 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.716 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.690 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.808 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.693 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.657 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.624 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.587 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.676 |
MOD_OFUCOSY | 158 | 165 | PF10250 | 0.668 |
MOD_PK_1 | 350 | 356 | PF00069 | 0.608 |
MOD_PKA_1 | 457 | 463 | PF00069 | 0.682 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.594 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.760 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.666 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.682 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.601 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.651 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.749 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.708 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.754 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.735 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.672 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.602 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.739 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.745 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.716 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.531 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.709 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.711 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.604 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.801 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.655 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.654 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.684 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.713 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 428 | 431 | PF00400 | 0.703 |
TRG_NLS_MonoCore_2 | 3 | 8 | PF00514 | 0.716 |
TRG_NLS_MonoCore_2 | 391 | 396 | PF00514 | 0.621 |
TRG_NLS_MonoExtC_3 | 9 | 14 | PF00514 | 0.713 |
TRG_NLS_MonoExtN_4 | 390 | 396 | PF00514 | 0.661 |
TRG_NLS_MonoExtN_4 | 4 | 9 | PF00514 | 0.768 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I8Z9 | Leishmania donovani | 80% | 100% |
A4H6F1 | Leishmania braziliensis | 65% | 100% |
A4HUU5 | Leishmania infantum | 80% | 100% |
E9ANI0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |