Align Serine uptake transporter, SerP1, of 259 aas and 12 TMSs (Trip et al. 2013). L-serine is the highest affinity substrate (Km = 18 μM), but SerP1 also transports L-threonine and L-cysteine (Km values = 20 - 40 μM) (characterized)
to candidate WP_038805943.1 HK29_RS02745 amino acid permease
Query= TCDB::F2HQ25 (459 letters) >NCBI__GCF_000382825.1:WP_038805943.1 Length = 445 Score = 448 bits (1152), Expect = e-130 Identities = 216/449 (48%), Positives = 305/449 (67%), Gaps = 10/449 (2%) Query: 11 QRGLQNRHIQLIAIAGTIGTGLFLGAGKTIQMTGPSVIFAYILIGIAMFFFLRTIGEMLY 70 +RGL NRH+Q++AIAGTIGTGLFLGAG++I +TGPS+I Y++ G MF +R +GEMLY Sbjct: 2 ERGLTNRHVQVMAIAGTIGTGLFLGAGRSISLTGPSIILIYMITGAFMFLMMRAVGEMLY 61 Query: 71 NDPSQHSFLNFVTKYSGVRTGYFTQWSYWLVIVFVCISELTAIGTYIQFWLPQVPLWLIE 130 DP QH+F+NF+T++ G GYF+ WSYWL +VF+ ++E+TAI Y+QFW P P WLI+ Sbjct: 62 QDPEQHTFINFITRHLGKGWGYFSVWSYWLSVVFIGMAEITAISHYVQFWFPSWPSWLIQ 121 Query: 131 IVMLALLFGLNTLNSRFFGETEFWFAMIKVAAIIGMIVTAIILVAGNFHYSTVLSGKTVH 190 IV L +L +N + + FGE EFWFAM+K+ AI+ MI T +V F +T H Sbjct: 122 IVFLTILALVNLIAVKLFGEVEFWFAMVKIVAILAMIATGAFMVLTGF--------ETSH 173 Query: 191 DSASLSNIFDGFQLFPHGAWNFVGALQMVMFAFTSMEFIGMTAAETVNPKKSLPKAINQI 250 +ASL+NI D F LFP+G NFV A QMV FA+ +EFIG+T +ET NP++ LPKA+ +I Sbjct: 174 GTASLANISDQFSLFPNGVMNFVMAFQMVFFAYLMIEFIGVTTSETKNPRQVLPKAVKEI 233 Query: 251 PVRILLFYVGALLAIMAIFNWHYIPADKSPFVMVFQLIGIKWAAALINFVVLTSAASALN 310 P+RI+ FY GALLAIM+I W + + SPFV VF+L GIKWAAALINFVVLTSAASALN Sbjct: 234 PLRIVFFYGGALLAIMSIIPWRELASSDSPFVTVFELAGIKWAAALINFVVLTSAASALN 293 Query: 311 SSLFSATRNMYSLAQQHDKGRLTPF--TKLSKAGIPINALYMATALSLLAPVLTLIPQIK 368 S+L+S R++Y +A L LS+ +P NA+ + L LA + ++P + Sbjct: 294 STLYSTGRHLYQIAHDSPNRFLKAIKADTLSRHNVPQNAIIASAILIALAAFINVLPGVS 353 Query: 369 NAFDFAASCTTNLFLVVYFITLYTYWQYRKSEDYNPKGFLTPKPQITVPFIVAIFAIVFA 428 +AF + ++ +++ +Y + + + +YRKS+D+ G+L P+ ++ P + F VFA Sbjct: 354 DAFALITASSSGVYIAIYILIMVAHLKYRKSQDFMADGYLMPQYRLLNPLTILFFIFVFA 413 Query: 429 SLFFNADTFYPALGAIVWTIFFGLYSHYK 457 +LF TF A+G+ +W I FG+YS +K Sbjct: 414 TLFLQESTFMGAVGSAIWIIGFGIYSQWK 442 Lambda K H 0.329 0.141 0.434 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: 643 Number of extensions: 26 Number of successful extensions: 3 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: 459 Length of database: 445 Length adjustment: 33 Effective length of query: 426 Effective length of database: 412 Effective search space: 175512 Effective search space used: 175512 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