Align Gamma aminobutyrate transaminase 1, mitochondrial; Gamma-aminobutyrate transaminase isozyme 1; LeGABA-TP1; SlGABA-T1; EC 2.6.1.96 (characterized)
to candidate WP_106709080.1 CU102_RS00900 aminotransferase class III-fold pyridoxal phosphate-dependent enzyme
Query= SwissProt::Q84P54 (515 letters) >NCBI__GCF_003010955.1:WP_106709080.1 Length = 464 Score = 438 bits (1126), Expect = e-127 Identities = 209/444 (47%), Positives = 304/444 (68%), Gaps = 1/444 (0%) Query: 67 HDMLAPFTAGWQSTDVDPLIIEKSEGSHVYDMQGRKYIDTLAGLWCTALGGNEPRLVDAA 126 + +L P+T + + PL++ +G +++D QG++YI+ ++GLWC LG + +++AA Sbjct: 16 NSVLHPYTPLHKLAETGPLVMGHGKGVYLFDTQGKEYIEGMSGLWCAGLGYGDEEMIEAA 75 Query: 127 TKQLNTLPFYHSFWNRTTKPSLDLAKELLDMFTAKKMAKAFFTNSGSEANDTQVKLVWYY 186 +Q+ TLP+YH F + +P+++LA++L ++ ++K F+T+SGSEANDTQVKL WYY Sbjct: 76 NEQMRTLPYYHLFGGKGMEPAIELAEKLKEIAPVP-ISKVFYTSSGSEANDTQVKLAWYY 134 Query: 187 NNALGRPNKKKFIARAKAYHGSTLISASLTGLPALHQNFDLPAPFVLHTDCPHYWRYHLP 246 NN LGRP KKK I+R KAYHG T+++ASLTGLP H+ +DLP VLHTDCPH++R+ Sbjct: 135 NNVLGRPKKKKIISRVKAYHGVTVMAASLTGLPGNHKGWDLPVSGVLHTDCPHFYRFGQE 194 Query: 247 GETEEEFSTRLAKNLEDLILKEGPETIAAFIAEPVMGAGGVIPPPATYFDKIQAVVKKYD 306 GE+E EF RLAK+L D+I +EGPETIAAFIAEPVMGAGGVI PP+ YF I+ +++++D Sbjct: 195 GESEAEFVARLAKSLIDMIEREGPETIAAFIAEPVMGAGGVIVPPSGYFAAIEPILREHD 254 Query: 307 ILFIADEVICAFGRLGTMFGSDMYNIKPDLVTLAKALSSAYMPIGAVLVSPEVSDVIHSQ 366 IL IADEVI FGR G +GS + P ++ AK L++AY P+GAVLV ++ Sbjct: 255 ILIIADEVINGFGRTGNWWGSQTVGMTPTTISAAKQLTAAYAPLGAVLVPEDLYQAYVDH 314 Query: 367 SNKLGSFSHGFTYSGHPVACAVALEAIKIYKERNMVERVNRISPKFQEGLKAFSDSPIIG 426 S ++G+F HGFTY GHPV CA+ ++AI+IY+ RN+VE V ++P F+ L D P++G Sbjct: 315 SAQIGTFGHGFTYGGHPVGCALGIKAIEIYQRRNIVEYVRGLTPTFEARLNKIKDHPLVG 374 Query: 427 EIRGLGLILATEFANNKSPNDHFPPEWGVGAYFGAQCQKNGMLVRVAGDTIMMSPPFVVT 486 E+R GL+ A E +K+ F P GVG+ + +G ++R GDTI PP ++T Sbjct: 375 EVRSCGLVGAVELVADKTTKRSFDPAHGVGSNLVKFLEGHGAILRALGDTIAFCPPMIIT 434 Query: 487 PEELDELIRIYGKALRETEKRVEE 510 +EL+EL + AL +TE V + Sbjct: 435 EDELNELFNRFELALADTEAYVSK 458 Lambda K H 0.318 0.135 0.402 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: 654 Number of extensions: 21 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: 515 Length of database: 464 Length adjustment: 34 Effective length of query: 481 Effective length of database: 430 Effective search space: 206830 Effective search space used: 206830 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 52 (24.6 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