Align Serine transporter, SerP2 or YdgB, of 459 aas and 12 TMSs (Trip et al. 2013). Transports L-alanine (Km = 20 μM), D-alanine (Km = 38 μM), L-serine, D-serine (Km = 356 μM) and glycine (Noens and Lolkema 2015). The encoding gene is adjacent to the one encoding SerP1 (TC# 2.A.3.1.21) (characterized)
to candidate WP_038805943.1 HK29_RS02745 amino acid permease
Query= TCDB::F2HQ24 (457 letters) >NCBI__GCF_000382825.1:WP_038805943.1 Length = 445 Score = 477 bits (1227), Expect = e-139 Identities = 221/441 (50%), Positives = 320/441 (72%), Gaps = 2/441 (0%) Query: 13 QRGLKNRHIQLIAIAGTIGTGLFLGAGKSIHLTGPSIIFVYLIIGALMYILLRAIGEMLY 72 +RGL NRH+Q++AIAGTIGTGLFLGAG+SI LTGPSII +Y+I GA M++++RA+GEMLY Sbjct: 2 ERGLTNRHVQVMAIAGTIGTGLFLGAGRSISLTGPSIILIYMITGAFMFLMMRAVGEMLY 61 Query: 73 QDPNQHSFLNFVSRYLGEKPGYFIQWSYLLVVVFVAMAELIAIGTYINFWLPDLPIWMTE 132 QDP QH+F+NF++R+LG+ GYF WSY L VVF+ MAE+ AI Y+ FW P P W+ + Sbjct: 62 QDPEQHTFINFITRHLGKGWGYFSVWSYWLSVVFIGMAEITAISHYVQFWFPSWPSWLIQ 121 Query: 133 VFVLVLLTLLNTLNPKFFGETEFWFGMIKIVAIIGLILTAIILIFSHYHTGTDTVSVTNI 192 + L +L L+N + K FGE EFWF M+KIVAI+ +I T ++ + + T T S+ NI Sbjct: 122 IVFLTILALVNLIAVKLFGEVEFWFAMVKIVAILAMIATGAFMVLTGFETSHGTASLANI 181 Query: 193 TKGFEFFPNGLSNFFESFQMVMFAFVSMEFIGMTAAETDNPRPTLKKAINQIPIRIVLFY 252 + F FPNG+ NF +FQMV FA++ +EFIG+T +ET NPR L KA+ +IP+RIV FY Sbjct: 182 SDQFSLFPNGVMNFVMAFQMVFFAYLMIEFIGVTTSETKNPRQVLPKAVKEIPLRIVFFY 241 Query: 253 VGALLAIMSIYQWRDIPADKSPFVTIFQLIGIKWAAALVNFVVLTSAASALNSALFSITR 312 GALLAIMSI WR++ + SPFVT+F+L GIKWAAAL+NFVVLTSAASALNS L+S R Sbjct: 242 GGALLAIMSIIPWRELASSDSPFVTVFELAGIKWAAALINFVVLTSAASALNSTLYSTGR 301 Query: 313 NLYSLSKLNNDKILKPF--TKFSKAGVPVNALLFTSLLILFTPFISMIPAISNSFVFITS 370 +LY ++ + ++ LK S+ VP NA++ +++LI FI+++P +S++F IT+ Sbjct: 302 HLYQIAHDSPNRFLKAIKADTLSRHNVPQNAIIASAILIALAAFINVLPGVSDAFALITA 361 Query: 371 VATNLFLVVYLMTLITYLKYRKSSDFDPKGFVLPAAHIFIPLAIAGFVLIFISLFCFKDT 430 ++ +++ +Y++ ++ +LKYRKS DF G+++P + PL I F+ +F +LF + T Sbjct: 362 SSSGVYIAIYILIMVAHLKYRKSQDFMADGYLMPQYRLLNPLTILFFIFVFATLFLQEST 421 Query: 431 IVPAIGSVIWVLIFGLFTFFK 451 + A+GS IW++ FG+++ +K Sbjct: 422 FMGAVGSAIWIIGFGIYSQWK 442 Lambda K H 0.330 0.144 0.431 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 611 Number of extensions: 22 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 457 Length of database: 445 Length adjustment: 33 Effective length of query: 424 Effective length of database: 412 Effective search space: 174688 Effective search space used: 174688 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory