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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4Q498
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 280 | 282 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.580 |
CLV_PCSK_FUR_1 | 189 | 193 | PF00082 | 0.656 |
CLV_PCSK_FUR_1 | 281 | 285 | PF00082 | 0.680 |
CLV_PCSK_FUR_1 | 288 | 292 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 337 | 339 | PF00082 | 0.545 |
CLV_PCSK_PC7_1 | 283 | 289 | PF00082 | 0.687 |
CLV_PCSK_PC7_1 | 29 | 35 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.799 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.503 |
DEG_APCC_DBOX_1 | 144 | 152 | PF00400 | 0.572 |
DEG_APCC_DBOX_1 | 178 | 186 | PF00400 | 0.654 |
DEG_APCC_DBOX_1 | 204 | 212 | PF00400 | 0.576 |
DEG_SPOP_SBC_1 | 420 | 424 | PF00917 | 0.691 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.592 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.636 |
DOC_MAPK_gen_1 | 142 | 151 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 191 | 201 | PF00069 | 0.686 |
DOC_MAPK_gen_1 | 350 | 360 | PF00069 | 0.650 |
DOC_MAPK_JIP1_4 | 195 | 201 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 45 | 53 | PF00069 | 0.580 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.557 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.598 |
LIG_14-3-3_CanoR_1 | 179 | 183 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 223 | 228 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 243 | 247 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 45 | 53 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 60 | 68 | PF00244 | 0.484 |
LIG_Actin_WH2_2 | 321 | 339 | PF00022 | 0.534 |
LIG_Actin_WH2_2 | 367 | 383 | PF00022 | 0.692 |
LIG_BIR_III_4 | 438 | 442 | PF00653 | 0.562 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 54 | 58 | PF00533 | 0.585 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.579 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.608 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.711 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.585 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.630 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.684 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.656 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.600 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.561 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.594 |
LIG_LIR_Gen_1 | 10 | 17 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 140 | 151 | PF02991 | 0.709 |
LIG_LIR_Nem_3 | 10 | 15 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.724 |
LIG_PDZ_Class_2 | 543 | 548 | PF00595 | 0.605 |
LIG_Pex14_2 | 7 | 11 | PF04695 | 0.572 |
LIG_PTAP_UEV_1 | 497 | 502 | PF05743 | 0.639 |
LIG_SH3_2 | 376 | 381 | PF14604 | 0.683 |
LIG_SH3_2 | 498 | 503 | PF14604 | 0.687 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.636 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.603 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.595 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.679 |
LIG_SH3_3 | 490 | 496 | PF00018 | 0.740 |
LIG_TRAF2_2 | 432 | 437 | PF00917 | 0.547 |
MOD_CDK_SPK_2 | 137 | 142 | PF00069 | 0.519 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.607 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.502 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.470 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.725 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.760 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.661 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.643 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.619 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.639 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.610 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.711 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.749 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.602 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.586 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.672 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.576 |
MOD_DYRK1A_RPxSP_1 | 338 | 342 | PF00069 | 0.620 |
MOD_GlcNHglycan | 100 | 104 | PF01048 | 0.443 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.651 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.571 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.571 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.649 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.652 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.679 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.643 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.754 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.672 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.737 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.635 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.535 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.549 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.596 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.630 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.530 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.580 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.659 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.758 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.583 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.637 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.590 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.635 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.753 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.654 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.735 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.559 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.643 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.581 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.594 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.565 |
MOD_N-GLC_1 | 74 | 79 | PF02516 | 0.560 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.555 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.635 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.562 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.629 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.694 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.517 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.650 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.531 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.610 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.632 |
MOD_NEK2_2 | 106 | 111 | PF00069 | 0.434 |
MOD_NEK2_2 | 367 | 372 | PF00069 | 0.554 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.624 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.561 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.613 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.674 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.621 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.458 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.604 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.533 |
MOD_PKA_1 | 286 | 292 | PF00069 | 0.688 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.617 |
MOD_PKA_1 | 337 | 343 | PF00069 | 0.546 |
MOD_PKA_1 | 350 | 356 | PF00069 | 0.520 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.618 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.593 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.542 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.597 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.570 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.688 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.617 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.556 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.696 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.567 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.458 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.686 |
MOD_PKB_1 | 284 | 292 | PF00069 | 0.687 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.602 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.541 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.722 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.607 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.566 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.640 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.715 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.715 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.591 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.580 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.663 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.599 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.667 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.715 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.572 |
TRG_NES_CRM1_1 | 41 | 52 | PF08389 | 0.552 |
TRG_NLS_Bipartite_1 | 280 | 294 | PF00514 | 0.636 |
TRG_NLS_MonoCore_2 | 289 | 294 | PF00514 | 0.562 |
TRG_NLS_MonoExtC_3 | 289 | 294 | PF00514 | 0.637 |
TRG_NLS_MonoExtC_3 | 535 | 541 | PF00514 | 0.577 |
TRG_NLS_MonoExtN_4 | 287 | 294 | PF00514 | 0.639 |
TRG_PTS2 | 1 | 42 | PF00400 | 0.625 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6K5 | Leishmania donovani | 83% | 100% |
A4HLE8 | Leishmania braziliensis | 61% | 100% |
A4I8V7 | Leishmania infantum | 84% | 100% |
E9B3S6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |