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: A4I5L7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.569 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 393 | 395 | PF00082 | 0.627 |
CLV_PCSK_PC7_1 | 123 | 129 | PF00082 | 0.710 |
CLV_PCSK_PC7_1 | 226 | 232 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.538 |
CLV_Separin_Metazoa | 62 | 66 | PF03568 | 0.501 |
DEG_APCC_DBOX_1 | 163 | 171 | PF00400 | 0.510 |
DEG_APCC_DBOX_1 | 77 | 85 | PF00400 | 0.610 |
DOC_ANK_TNKS_1 | 35 | 42 | PF00023 | 0.567 |
DOC_CYCLIN_yClb3_PxF_3 | 245 | 253 | PF00134 | 0.595 |
DOC_MAPK_gen_1 | 230 | 238 | PF00069 | 0.724 |
DOC_MAPK_gen_1 | 448 | 456 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 76 | 83 | PF00069 | 0.608 |
DOC_MAPK_HePTP_8 | 359 | 371 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 230 | 238 | PF00069 | 0.617 |
DOC_MAPK_MEF2A_6 | 362 | 371 | PF00069 | 0.519 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.517 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.651 |
LIG_14-3-3_CanoR_1 | 164 | 174 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 408 | 416 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 71 | 79 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.527 |
LIG_BIR_III_4 | 336 | 340 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.650 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.575 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.773 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.536 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.508 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.555 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.382 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.533 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.681 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.619 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.694 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.616 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.587 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.747 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.642 |
LIG_LIR_Apic_2 | 168 | 174 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 312 | 320 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.584 |
LIG_LIR_LC3C_4 | 414 | 418 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.591 |
LIG_NRBOX | 234 | 240 | PF00104 | 0.620 |
LIG_PCNA_yPIPBox_3 | 523 | 533 | PF02747 | 0.553 |
LIG_PTAP_UEV_1 | 244 | 249 | PF05743 | 0.641 |
LIG_PTB_Apo_2 | 449 | 456 | PF02174 | 0.493 |
LIG_PTB_Phospho_1 | 449 | 455 | PF10480 | 0.491 |
LIG_SH2_CRK | 296 | 300 | PF00017 | 0.653 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.538 |
LIG_SH2_GRB2like | 332 | 335 | PF00017 | 0.593 |
LIG_SH2_PTP2 | 210 | 213 | PF00017 | 0.596 |
LIG_SH2_SRC | 315 | 318 | PF00017 | 0.531 |
LIG_SH2_SRC | 332 | 335 | PF00017 | 0.593 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.534 |
LIG_SH2_STAT3 | 398 | 401 | PF00017 | 0.671 |
LIG_SH2_STAT3 | 537 | 540 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.402 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.710 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.619 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.527 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.556 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.575 |
LIG_SH3_3 | 597 | 603 | PF00018 | 0.703 |
LIG_SH3_CIN85_PxpxPR_1 | 599 | 604 | PF14604 | 0.704 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.561 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.637 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.644 |
LIG_WW_3 | 599 | 603 | PF00397 | 0.701 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.664 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.651 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.474 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.631 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.595 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.609 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.600 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.625 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.565 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.668 |
MOD_CMANNOS | 151 | 154 | PF00535 | 0.468 |
MOD_Cter_Amidation | 162 | 165 | PF01082 | 0.515 |
MOD_Cter_Amidation | 31 | 34 | PF01082 | 0.583 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.614 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.613 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.506 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.701 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.607 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.682 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.639 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.553 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.636 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.628 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.524 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.577 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.651 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.654 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.744 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.675 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.727 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.619 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.496 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.477 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.618 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.598 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.660 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.546 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.704 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.775 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.757 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.596 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.667 |
MOD_NEK2_2 | 505 | 510 | PF00069 | 0.629 |
MOD_PIKK_1 | 176 | 182 | PF00454 | 0.547 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.664 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.551 |
MOD_PIKK_1 | 407 | 413 | PF00454 | 0.511 |
MOD_PK_1 | 496 | 502 | PF00069 | 0.632 |
MOD_PKA_1 | 127 | 133 | PF00069 | 0.692 |
MOD_PKA_1 | 303 | 309 | PF00069 | 0.593 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.677 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.692 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.626 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.605 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.595 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.683 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.586 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.533 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.437 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.691 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.580 |
MOD_Plk_2-3 | 399 | 405 | PF00069 | 0.620 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.465 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.578 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.599 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.649 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.578 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.613 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.621 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.645 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.660 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.595 |
TRG_DiLeu_BaEn_4 | 223 | 229 | PF01217 | 0.591 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.580 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.511 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.525 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.757 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 601 | 604 | PF00400 | 0.712 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 303 | 307 | PF00026 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 448 | 453 | PF00026 | 0.476 |
TRG_PTS1 | 602 | 605 | PF00515 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IRZ9 | Leishmania donovani | 99% | 100% |
A4HIC5 | Leishmania braziliensis | 70% | 100% |
E9B0W2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q7A4 | Leishmania major | 92% | 100% |