Align Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19) (characterized)
to candidate 5209240 Shew_1718 adenosylmethionine-8-amino-7-oxononanoate aminotransferase (RefSeq)
Query= reanno::SB2B:6938540 (460 letters) >FitnessBrowser__PV4:5209240 Length = 446 Score = 180 bits (456), Expect = 1e-49 Identities = 130/452 (28%), Positives = 214/452 (47%), Gaps = 32/452 (7%) Query: 16 DAAHHLHPFTDSADLAKRGTRVIERAEGVYIWDAKGNKLLDAMAGLWCVNVGYGRKSIAD 75 D H HP+T + AEG + G +L+D + W GYG I + Sbjct: 12 DRQHIWHPYTSMTQALP--VYGVVSAEGCELILDDGRRLIDGTSSWWACVHGYGHPYILE 69 Query: 76 AAYAQLQTLPFYNNFFQCTHEPAIRLASKIASLAPGHMNRVFFTGSGSEANDTNLRMVRR 135 A QL TL + F TH AI ++ K+ ++ ++ +VF SGS A + ++M + Sbjct: 70 AMQKQLSTLS-HVMFGGITHPSAIAVSKKLLAMTSDNLTKVFLADSGSIAVEVAMKMALQ 128 Query: 136 YWDLKGMPSKKTIISRKNAYHGSTVAGASL----GGMGFMHQQGDLPIPGIVHIDQPYWF 191 YW +G PSK+ I++ K+ YHG T A S+ GGM M + + Q + Sbjct: 129 YWQGRGAPSKQRILTVKHGYHGDTFAAMSVCDPEGGMHTMFGEA---------VTQQLFA 179 Query: 192 GEGRDMSPEAFGIKTAQALEAKILELGEDKVAAFIAEPF-QGAGGVIIPPDSYWNEIKRI 250 + E +A+EA +L +AA I EP QGAG + Y ++ + Sbjct: 180 PAPKTPFGETLIADDLEAMEA-LLNAHHQTIAAVIIEPIMQGAGAMHFYSADYLKGLRAL 238 Query: 251 LEKYNILFILDEVISGFGRTGNWFAAQTLGLKPDLITIAKGMTSGYIPMGGVIVSDRVA- 309 ++Y +L ILDE+ +GFGRTG FA Q G++ D++ + K +T GYI + + SD VA Sbjct: 239 CDRYKVLLILDEIATGFGRTGKLFAYQHAGIEADILCLGKALTGGYISLAATLCSDEVAL 298 Query: 310 DVLISDGGEFAHGFTYSGHPVAAAVALENIRILEEERLVDKVRTDTGPYLQDRLQTLSAH 369 + S G F HG T+ G+P+A A A ++ ++ + + ++V ++ L T SA Sbjct: 299 GISDSPSGVFMHGPTFMGNPLACAAASASLDLINQHQWPEQVAA-IEQQMKQELATASAI 357 Query: 370 PLVGEVRGMGMVGAIELVADKHSMVRFGSEISAGMLCREACIESGLVMRAVGDTMIISPP 429 V VR +G VG IE+ ++ ++A ++ G+ +R + I PP Sbjct: 358 EGVKAVRCLGAVGVIEMTRSVNTAA-----------LQQAFVDRGVWVRPFSSYIYIMPP 406 Query: 430 LCITRDEIDELIFKASQALSLT-LEKIAARGN 460 I+ ++ L + ++ E A+RG+ Sbjct: 407 YTISAQQLSRLTQAMLEVAAIAGAEAKASRGD 438 Lambda K H 0.321 0.137 0.408 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: 520 Number of extensions: 32 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: 460 Length of database: 446 Length adjustment: 33 Effective length of query: 427 Effective length of database: 413 Effective search space: 176351 Effective search space used: 176351 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (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