Membrane associated proteins, A44l -like
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4IDZ9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 19 |
GO:0003824 | catalytic activity | 1 | 19 |
GO:0005488 | binding | 1 | 19 |
GO:0005524 | ATP binding | 5 | 19 |
GO:0016462 | pyrophosphatase activity | 5 | 19 |
GO:0016787 | hydrolase activity | 2 | 19 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 19 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 19 |
GO:0016887 | ATP hydrolysis activity | 7 | 19 |
GO:0017076 | purine nucleotide binding | 4 | 19 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 19 |
GO:0030554 | adenyl nucleotide binding | 5 | 19 |
GO:0032553 | ribonucleotide binding | 3 | 19 |
GO:0032555 | purine ribonucleotide binding | 4 | 19 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 19 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 19 |
GO:0036094 | small molecule binding | 2 | 19 |
GO:0043167 | ion binding | 2 | 19 |
GO:0043168 | anion binding | 3 | 19 |
GO:0097159 | organic cyclic compound binding | 2 | 19 |
GO:0097367 | carbohydrate derivative binding | 2 | 19 |
GO:1901265 | nucleoside phosphate binding | 3 | 19 |
GO:1901363 | heterocyclic compound binding | 2 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 628 | 632 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 695 | 699 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.446 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.309 |
CLV_PCSK_PC7_1 | 318 | 324 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.532 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.536 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.753 |
DEG_SCF_SKP2-CKS1_1 | 557 | 564 | PF00560 | 0.637 |
DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.443 |
DOC_CKS1_1 | 677 | 682 | PF01111 | 0.642 |
DOC_CKS1_1 | 96 | 101 | PF01111 | 0.214 |
DOC_CYCLIN_yClb1_LxF_4 | 307 | 312 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 165 | 171 | PF00134 | 0.611 |
DOC_MAPK_gen_1 | 130 | 138 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.599 |
DOC_MAPK_gen_1 | 204 | 211 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 517 | 527 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 162 | 171 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 204 | 211 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 335 | 342 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 307 | 313 | PF00149 | 0.516 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.529 |
DOC_PP1_RVXF_1 | 615 | 621 | PF00149 | 0.633 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.595 |
DOC_PP2B_LxvP_1 | 2 | 5 | PF13499 | 0.590 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.326 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 676 | 681 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.214 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 468 | 472 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 480 | 490 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 520 | 529 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 669 | 675 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 705 | 714 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 71 | 78 | PF00244 | 0.371 |
LIG_Actin_WH2_2 | 2 | 17 | PF00022 | 0.668 |
LIG_APCC_ABBA_1 | 158 | 163 | PF00400 | 0.568 |
LIG_BIR_III_4 | 463 | 467 | PF00653 | 0.659 |
LIG_BRCT_BRCA1_1 | 672 | 676 | PF00533 | 0.578 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.370 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.631 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.474 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.402 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.283 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.614 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.511 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.458 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.527 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.699 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.638 |
LIG_Integrin_RGD_1 | 347 | 349 | PF01839 | 0.243 |
LIG_LIR_Apic_2 | 140 | 145 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 93 | 99 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 206 | 214 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 365 | 376 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 528 | 536 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 673 | 680 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.749 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 45 | 50 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 528 | 532 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 673 | 677 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.266 |
LIG_NRBOX | 309 | 315 | PF00104 | 0.434 |
LIG_NRBOX | 482 | 488 | PF00104 | 0.570 |
LIG_PCNA_PIPBox_1 | 135 | 144 | PF02747 | 0.525 |
LIG_PTB_Apo_2 | 128 | 135 | PF02174 | 0.613 |
LIG_RPA_C_Fungi | 17 | 29 | PF08784 | 0.408 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.553 |
LIG_SH2_CRK | 674 | 678 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.545 |
LIG_SH2_PTP2 | 529 | 532 | PF00017 | 0.338 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.323 |
LIG_SH3_1 | 96 | 102 | PF00018 | 0.233 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.527 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.419 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.540 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.464 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.463 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.683 |
LIG_SH3_3 | 559 | 565 | PF00018 | 0.693 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.252 |
LIG_SH3_4 | 429 | 436 | PF00018 | 0.562 |
LIG_SUMO_SIM_anti_2 | 495 | 504 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 53 | 58 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 137 | 143 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 500 | 506 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 587 | 594 | PF11976 | 0.526 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.467 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.752 |
LIG_TRAF2_1 | 656 | 659 | PF00917 | 0.443 |
LIG_UBA3_1 | 110 | 117 | PF00899 | 0.351 |
LIG_UBA3_1 | 135 | 144 | PF00899 | 0.563 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.394 |
MOD_CDK_SPxK_1 | 558 | 564 | PF00069 | 0.562 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.549 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.267 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.193 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.687 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.664 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.586 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.744 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.364 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.693 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.526 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.443 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.567 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.484 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.444 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.735 |
MOD_Cter_Amidation | 320 | 323 | PF01082 | 0.394 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.514 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.477 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.681 |
MOD_GlcNHglycan | 575 | 579 | PF01048 | 0.703 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.651 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.453 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.564 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.526 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.628 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.535 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.249 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.335 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.518 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.748 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.729 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.675 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.538 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.547 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.488 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.538 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.342 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.543 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.534 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.353 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.498 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.339 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.562 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.542 |
MOD_NEK2_2 | 203 | 208 | PF00069 | 0.393 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.695 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.562 |
MOD_PIKK_1 | 660 | 666 | PF00454 | 0.437 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.442 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.496 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.394 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.564 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.709 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.486 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.464 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.543 |
MOD_PKA_2 | 670 | 676 | PF00069 | 0.406 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.494 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.380 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.433 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.430 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.422 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.398 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.270 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.571 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.336 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.381 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.433 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.581 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.599 |
MOD_ProDKin_1 | 676 | 682 | PF00069 | 0.433 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.233 |
TRG_DiLeu_BaEn_1 | 19 | 24 | PF01217 | 0.410 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.274 |
TRG_DiLeu_BaEn_1 | 531 | 536 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_2 | 154 | 160 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_4 | 366 | 372 | PF01217 | 0.274 |
TRG_DiLeu_LyEn_5 | 19 | 24 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.521 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 674 | 677 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.508 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P906 | Leptomonas seymouri | 46% | 98% |
A0A1X0NTT2 | Trypanosomatidae | 33% | 100% |
A0A3Q8IC80 | Leishmania donovani | 28% | 97% |
A0A3Q8IC95 | Leishmania donovani | 28% | 100% |
A0A3Q8IHZ0 | Leishmania donovani | 100% | 100% |
A0A422NUH1 | Trypanosoma rangeli | 30% | 100% |
A4HCE5 | Leishmania braziliensis | 27% | 96% |
A4HZW7 | Leishmania infantum | 28% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9AVS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 98% |
Q4Q0H4 | Leishmania major | 90% | 100% |
Q4QBQ3 | Leishmania major | 29% | 100% |
Q4QBQ4 | Leishmania major | 29% | 100% |
V5D9P2 | Trypanosoma cruzi | 27% | 100% |
V5DMJ8 | Trypanosoma cruzi | 30% | 100% |