Align Gamma-aminobutyrate:alpha-ketoglutarate aminotransferase (EC 2.6.1.19) (characterized)
to candidate BPHYT_RS30220 BPHYT_RS30220 hypothetical protein
Query= reanno::SB2B:6938540 (460 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS30220 BPHYT_RS30220 hypothetical protein Length = 465 Score = 346 bits (888), Expect = e-100 Identities = 195/456 (42%), Positives = 268/456 (58%), Gaps = 11/456 (2%) Query: 9 ISALQAMDAAHHLHPFTDSADLAKRGTRVIERAEGVYIWDAKGNKLLDAMAGLWCVNVGY 68 I +L D H +HP + RG V+E A G ++ DA GN+LLDA +GLWCVNVGY Sbjct: 3 IQSLIEADRKHLIHPVINYRAHEARGVTVLESASGAFLRDAAGNELLDAFSGLWCVNVGY 62 Query: 69 GRKSIADAAYAQLQTLPFYNNFFQCTHEPAIRLASKIASLAPGHMNRVFFTGSGSEANDT 128 G++SI DAA AQ+Q LP+ +F EPAI LA K+ ++P + V+FT GS+A D+ Sbjct: 63 GQQSIVDAATAQMQKLPYATGYFHFGSEPAIELAQKLVEVSPASLQHVYFTLGGSDAVDS 122 Query: 129 NLRMVRRYWDLKGMPSKKTIISRKNAYHGSTVAGASLGGMGFMHQQGDLPIPGIVHIDQP 188 LR + Y++ G PSKK II+ + YHGS+ GA L + H+ DLP+P H+ P Sbjct: 123 ALRFITHYFNSTGRPSKKHIIALQRGYHGSSTTGAGLTALPAFHRNFDLPLPNQHHLPSP 182 Query: 189 YWFGEGRDMSPEAFGI-KTAQALEAKILELGEDKVAAFIAEPFQGAGGVIIPPDSYWNEI 247 Y + D + +A I + ALEAK+ ELG D VAAF EP QG+GGVI+PP + + Sbjct: 183 YAY--RNDFADDAALIAASVAALEAKVAELGADNVAAFFCEPIQGSGGVIVPPVGWLKAM 240 Query: 248 KRILEKYNILFILDEVISGFGRTGNWFAAQTLGLKPDLITIAKGMTSGYIPMGGVIVSDR 307 + K ILF+ DEVI+GFGRTG FA Q ++PDL+T+AKG+T+GY PMG V++SD Sbjct: 241 RESCRKLGILFVADEVITGFGRTGPLFACQGENVEPDLMTVAKGLTAGYAPMGAVLMSDE 300 Query: 308 VADVLISDGGE--FAHGFTYSGHPVAAAVALENIRILEEERLVDKVRTDTGPYLQDRLQT 365 + + E HG TYS HPV+AA+ LE +R+ E L+ P L Sbjct: 301 IYQGIADSHAEAVVGHGHTYSAHPVSAAIGLEVLRLYHEGGLLAN-GVARAPRFARGLDA 359 Query: 366 LSAHPLVGEVRGMGMVGAIELVADKHSMVRFGSEISAGMLCREACIESGLVMRAVGDTMI 425 L AHPLVG+ R G++GA+ELVADK S F + A E+ L+ RA GD ++ Sbjct: 360 LLAHPLVGDSRHRGLLGALELVADKDSKAGFDPALKLSERIAAAAYENRLIFRAFGDNIL 419 Query: 426 -ISPPLCITRDEIDELIFKASQALSLTLEKIAARGN 460 +P L T E D L+F + L TL+ + A+ + Sbjct: 420 GFAPALSYTEAEFD-LMF---ERLEKTLDDVLAQAD 451 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: 551 Number of extensions: 18 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: 465 Length adjustment: 33 Effective length of query: 427 Effective length of database: 432 Effective search space: 184464 Effective search space used: 184464 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 preprint 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