Align D-serine/D-alanine/glycine transporter (characterized)
to candidate BWI76_RS06245 BWI76_RS06245 proline-specific permease ProY
Query= SwissProt::A0A0H2VDI7 (470 letters) >FitnessBrowser__Koxy:BWI76_RS06245 Length = 456 Score = 374 bits (960), Expect = e-108 Identities = 192/449 (42%), Positives = 282/449 (62%), Gaps = 10/449 (2%) Query: 15 AEQSLRRNLTNRHIQLIAIGGAIGTGLFMGSGKTISLAGPSIIFVYMIIGFMLFFVMRAM 74 + L+R L+ RHI+ +A+G AIGTGLF GS I +AGPS++ Y+I G + +MRA+ Sbjct: 3 SSNKLKRGLSTRHIRFMALGSAIGTGLFYGSADAIKMAGPSVLLAYIIGGVAAYIIMRAL 62 Query: 75 GELLLSNLEYKSFSDFASDLLGPWAGYFTGWTYWFCWVVTGMADVVAITAYAQFWFPGLS 134 GE+ + N SFS +A D LGP AGY TGWTY F ++ +ADV A Y WFP + Sbjct: 63 GEMSVHNPAASSFSRYAQDYLGPLAGYITGWTYCFEILIVAIADVTAFGIYMGVWFPAVP 122 Query: 135 DWVASLSVIILLLVLNLATVKMFGEMEFWFAMIKIVAIVSLIVVGLVMVAMHFQS---PT 191 WV LSV++++ +NL +VK+FGE+EFWF+ K+ I+ +I+ G ++ + PT Sbjct: 123 HWVWVLSVVLIICAVNLMSVKVFGELEFWFSFFKVATIIIMILAGFGIIIWGIGNGGQPT 182 Query: 192 GVEASFAHLWNDGGWFPKGLSGFFAGFQIAVFAFVGIELVGTTAAETKDPEKSLPRAINS 251 G+ +LW++GG+F G G Q+ +FA+ GIE++G TA E KDPEKS+PRAINS Sbjct: 183 GIH----NLWSNGGFFSNGWLGMVMSLQMVMFAYGGIEIIGITAGEAKDPEKSIPRAINS 238 Query: 252 IPIRIIMFYVFSLIVIMSVTPWSSVVPEKSPFVELFVLVGLPAAASVINFVVLTSAASSA 311 +P+RI++FYV +L VIMS+ PW+ V SPFV F +G+ AAS++NFVVLT++ S+ Sbjct: 239 VPMRILVFYVGTLFVIMSIYPWNQVGTNGSPFVLTFQHLGITFAASILNFVVLTASLSAI 298 Query: 312 NSGVFSTSRMLFGLAQEGVAPKAFAKLSKRAVPAKGLTFSCICLLGGVVMLYVNPSVIGA 371 NS VF RML G+A++G APK FAK S+R VP + I LL V + Y+ P Sbjct: 299 NSDVFGVGRMLHGMAEQGSAPKMFAKTSRRGVPWVTVMVMTIALLFAVYLNYIMPE--NV 356 Query: 372 FTMITTVSAILFMFVWTIILCSYLVYRKQRPHLHEKSI-YKMPLGKLMCWVCMAFFVFVL 430 F +I +++ ++VW +IL S + +R++ P K++ +K+P G + + F VF++ Sbjct: 357 FLVIASLATFATVWVWIMILLSQIAFRRRLPPEEAKALKFKVPGGVTTTVIGLLFLVFII 416 Query: 431 VLLTLEDDTRQALLVTPLWFIALGLGWLF 459 L+ DTR +L V W I L +GW F Sbjct: 417 GLIGYHPDTRISLYVGFAWIILLLIGWQF 445 Lambda K H 0.329 0.141 0.441 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: 665 Number of extensions: 42 Number of successful extensions: 4 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: 470 Length of database: 456 Length adjustment: 33 Effective length of query: 437 Effective length of database: 423 Effective search space: 184851 Effective search space used: 184851 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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