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: A4HX04
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.778 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.759 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.757 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.800 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 616 | 618 | PF00675 | 0.642 |
CLV_PCSK_FUR_1 | 270 | 274 | PF00082 | 0.786 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.800 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.731 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.803 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.795 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.744 |
DEG_SCF_TRCP1_1 | 608 | 614 | PF00400 | 0.742 |
DOC_ANK_TNKS_1 | 566 | 573 | PF00023 | 0.722 |
DOC_MAPK_DCC_7 | 118 | 126 | PF00069 | 0.718 |
DOC_MAPK_gen_1 | 335 | 345 | PF00069 | 0.759 |
DOC_MAPK_gen_1 | 599 | 605 | PF00069 | 0.704 |
DOC_PP2B_LxvP_1 | 441 | 444 | PF13499 | 0.774 |
DOC_PP2B_LxvP_1 | 580 | 583 | PF13499 | 0.751 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.842 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.859 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.784 |
DOC_USP7_MATH_2 | 243 | 249 | PF00917 | 0.746 |
DOC_USP7_UBL2_3 | 513 | 517 | PF12436 | 0.721 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.676 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.813 |
LIG_14-3-3_CanoR_1 | 107 | 113 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 173 | 182 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 229 | 236 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 285 | 295 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 458 | 462 | PF00244 | 0.779 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.827 |
LIG_14-3-3_CanoR_1 | 573 | 583 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 599 | 606 | PF00244 | 0.776 |
LIG_CtBP_PxDLS_1 | 131 | 135 | PF00389 | 0.593 |
LIG_deltaCOP1_diTrp_1 | 387 | 395 | PF00928 | 0.762 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.856 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.815 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.650 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.831 |
LIG_GSK3_LRP6_1 | 581 | 587 | PF00069 | 0.753 |
LIG_Integrin_isoDGR_2 | 615 | 617 | PF01839 | 0.757 |
LIG_LIR_Apic_2 | 135 | 141 | PF02991 | 0.760 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.757 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.654 |
LIG_SH2_GRB2like | 412 | 415 | PF00017 | 0.757 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.585 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.759 |
LIG_SH3_1 | 163 | 169 | PF00018 | 0.742 |
LIG_SH3_1 | 233 | 239 | PF00018 | 0.841 |
LIG_SH3_1 | 96 | 102 | PF00018 | 0.772 |
LIG_SH3_2 | 625 | 630 | PF14604 | 0.800 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.815 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.789 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.567 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.775 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.842 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.824 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.677 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.471 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.645 |
LIG_SH3_3 | 622 | 628 | PF00018 | 0.804 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.834 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.772 |
LIG_SUMO_SIM_anti_2 | 42 | 48 | PF11976 | 0.689 |
LIG_TRAF2_1 | 250 | 253 | PF00917 | 0.660 |
LIG_TRFH_1 | 180 | 184 | PF08558 | 0.745 |
LIG_WW_3 | 335 | 339 | PF00397 | 0.615 |
MOD_CDC14_SPxK_1 | 183 | 186 | PF00782 | 0.702 |
MOD_CDK_SPxK_1 | 180 | 186 | PF00069 | 0.707 |
MOD_CDK_SPxxK_3 | 180 | 187 | PF00069 | 0.631 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.747 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.628 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.775 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.804 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.789 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.759 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.823 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.824 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.713 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.706 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.673 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.691 |
MOD_CK2_1 | 598 | 604 | PF00069 | 0.818 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.763 |
MOD_Cter_Amidation | 184 | 187 | PF01082 | 0.606 |
MOD_Cter_Amidation | 615 | 618 | PF01082 | 0.754 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.688 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.623 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.805 |
MOD_GlcNHglycan | 211 | 216 | PF01048 | 0.653 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.735 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.707 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.771 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.775 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.646 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.700 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.528 |
MOD_GlcNHglycan | 607 | 611 | PF01048 | 0.760 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.771 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.666 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.714 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.769 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.808 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.738 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.824 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.689 |
MOD_LATS_1 | 156 | 162 | PF00433 | 0.723 |
MOD_LATS_1 | 474 | 480 | PF00433 | 0.635 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.835 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.824 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.654 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.781 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.750 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.743 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.572 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.657 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.740 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.547 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.773 |
MOD_PIKK_1 | 495 | 501 | PF00454 | 0.792 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.801 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.676 |
MOD_PKA_1 | 173 | 179 | PF00069 | 0.734 |
MOD_PKA_1 | 285 | 291 | PF00069 | 0.754 |
MOD_PKA_1 | 516 | 522 | PF00069 | 0.775 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.789 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.794 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.735 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.617 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.828 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.574 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.637 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.788 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.625 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.818 |
MOD_PKB_1 | 257 | 265 | PF00069 | 0.617 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.726 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.827 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.674 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.756 |
MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.723 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.816 |
MOD_SUMO_rev_2 | 509 | 519 | PF00179 | 0.668 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.796 |
TRG_NLS_MonoExtN_4 | 514 | 521 | PF00514 | 0.792 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDQ3 | Leishmania donovani | 98% | 99% |
A4H8N4 | Leishmania braziliensis | 52% | 96% |
E9AQR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QEQ9 | Leishmania major | 84% | 100% |