Uncharacterized Protein, Uncharacterized
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: A4HTZ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 490 | 494 | PF00656 | 0.710 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.637 |
CLV_PCSK_FUR_1 | 196 | 200 | PF00082 | 0.643 |
CLV_PCSK_FUR_1 | 234 | 238 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 265 | 267 | PF00082 | 0.750 |
CLV_PCSK_PC7_1 | 352 | 358 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.566 |
DEG_APCC_DBOX_1 | 35 | 43 | PF00400 | 0.452 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.707 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.707 |
DEG_SPOP_SBC_1 | 457 | 461 | PF00917 | 0.647 |
DOC_CKS1_1 | 126 | 131 | PF01111 | 0.654 |
DOC_MAPK_gen_1 | 187 | 195 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 196 | 203 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 256 | 263 | PF00069 | 0.647 |
DOC_MAPK_gen_1 | 265 | 272 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.571 |
DOC_PP2B_LxvP_1 | 473 | 476 | PF13499 | 0.667 |
DOC_PP4_MxPP_1 | 367 | 370 | PF00568 | 0.737 |
DOC_SPAK_OSR1_1 | 308 | 312 | PF12202 | 0.744 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.534 |
DOC_USP7_MATH_2 | 392 | 398 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.741 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.702 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.793 |
LIG_14-3-3_CanoR_1 | 163 | 167 | PF00244 | 0.752 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 341 | 345 | PF00244 | 0.824 |
LIG_14-3-3_CanoR_1 | 478 | 482 | PF00244 | 0.773 |
LIG_Actin_WH2_2 | 97 | 113 | PF00022 | 0.560 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.709 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.657 |
LIG_CtBP_PxDLS_1 | 507 | 511 | PF00389 | 0.671 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.734 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.733 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.631 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.655 |
LIG_GBD_Chelix_1 | 31 | 39 | PF00786 | 0.637 |
LIG_LIR_Apic_2 | 376 | 381 | PF02991 | 0.696 |
LIG_LIR_Apic_2 | 404 | 408 | PF02991 | 0.602 |
LIG_LIR_Apic_2 | 501 | 507 | PF02991 | 0.694 |
LIG_LIR_Apic_2 | 97 | 101 | PF02991 | 0.728 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.782 |
LIG_SH2_CRK | 242 | 246 | PF00017 | 0.584 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.805 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.730 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.689 |
LIG_SH2_PTP2 | 405 | 408 | PF00017 | 0.601 |
LIG_SH2_PTP2 | 504 | 507 | PF00017 | 0.683 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.728 |
LIG_SH2_STAT3 | 155 | 158 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.683 |
LIG_SH3_2 | 6 | 11 | PF14604 | 0.670 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.749 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.637 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.663 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.720 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.616 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.595 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.659 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.539 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.751 |
LIG_SUMO_SIM_anti_2 | 27 | 34 | PF11976 | 0.497 |
LIG_SUMO_SIM_anti_2 | 509 | 514 | PF11976 | 0.674 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.669 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.626 |
LIG_TRAF2_1 | 438 | 441 | PF00917 | 0.623 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.665 |
LIG_WRC_WIRS_1 | 252 | 257 | PF05994 | 0.615 |
MOD_CDK_SPxK_1 | 298 | 304 | PF00069 | 0.646 |
MOD_CDK_SPxK_1 | 335 | 341 | PF00069 | 0.764 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.735 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.581 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.596 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.686 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.743 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.714 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.566 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.647 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.641 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.660 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.743 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.640 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.640 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.614 |
MOD_Cter_Amidation | 196 | 199 | PF01082 | 0.616 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.690 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.693 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.711 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.747 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.681 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.654 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.604 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.661 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.753 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.749 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.655 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.547 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.640 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.630 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.777 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.815 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.725 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.657 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.654 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.575 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.671 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.700 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.827 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.725 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.755 |
MOD_N-GLC_1 | 224 | 229 | PF02516 | 0.722 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.527 |
MOD_N-GLC_1 | 335 | 340 | PF02516 | 0.839 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.744 |
MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.664 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.699 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.768 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.658 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.673 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.725 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.660 |
MOD_PIKK_1 | 498 | 504 | PF00454 | 0.719 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.757 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.747 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.679 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.551 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.847 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.451 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.761 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.674 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.744 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.824 |
MOD_Plk_1 | 224 | 230 | PF00069 | 0.718 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.522 |
MOD_Plk_1 | 487 | 493 | PF00069 | 0.836 |
MOD_Plk_1 | 508 | 514 | PF00069 | 0.677 |
MOD_Plk_2-3 | 436 | 442 | PF00069 | 0.661 |
MOD_Plk_2-3 | 487 | 493 | PF00069 | 0.721 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.757 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.603 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.677 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.606 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.654 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.621 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.702 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.755 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.743 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.791 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.747 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.704 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.791 |
MOD_SUMO_rev_2 | 449 | 457 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 56 | 64 | PF00179 | 0.656 |
TRG_DiLeu_BaEn_4 | 240 | 246 | PF01217 | 0.579 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.630 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.804 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.442 |
TRG_NLS_MonoCore_2 | 416 | 421 | PF00514 | 0.635 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.681 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQN7 | Leishmania donovani | 100% | 100% |
A4H5Q1 | Leishmania braziliensis | 44% | 97% |
E9AMS1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QHV4 | Leishmania major | 76% | 89% |