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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7X488
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 70 | 74 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.614 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 531 | 533 | PF00082 | 0.459 |
CLV_PCSK_PC7_1 | 221 | 227 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.641 |
DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 327 | 335 | PF00400 | 0.545 |
DOC_CYCLIN_yCln2_LP_2 | 342 | 348 | PF00134 | 0.585 |
DOC_MAPK_gen_1 | 510 | 517 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 531 | 538 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 531 | 538 | PF00069 | 0.524 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.643 |
DOC_USP7_UBL2_3 | 463 | 467 | PF12436 | 0.616 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 180 | 189 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 204 | 212 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 225 | 234 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 244 | 249 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 307 | 315 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 389 | 396 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 404 | 412 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 421 | 427 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 452 | 457 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 628 | 633 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 99 | 107 | PF00244 | 0.753 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_2 | 90 | 96 | PF00533 | 0.686 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.559 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.576 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.646 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.634 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.602 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.647 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.584 |
LIG_FHA_2 | 509 | 515 | PF00498 | 0.566 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.618 |
LIG_Integrin_RGD_1 | 397 | 399 | PF01839 | 0.681 |
LIG_LIR_Gen_1 | 128 | 134 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.483 |
LIG_SH2_SRC | 545 | 548 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.454 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.570 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.620 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.493 |
LIG_SUMO_SIM_anti_2 | 427 | 433 | PF11976 | 0.636 |
LIG_SUMO_SIM_par_1 | 533 | 539 | PF11976 | 0.518 |
LIG_TRAF2_1 | 471 | 474 | PF00917 | 0.628 |
LIG_TRFH_1 | 320 | 324 | PF08558 | 0.634 |
MOD_CDK_SPK_2 | 259 | 264 | PF00069 | 0.683 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.634 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.684 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.558 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.552 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.751 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.592 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.676 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.543 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.588 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.506 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.662 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.637 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.651 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.608 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.533 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.676 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.488 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.598 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.704 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.586 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.706 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.662 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.557 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.641 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.601 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.628 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.631 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.685 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.777 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.719 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.703 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.591 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.641 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.613 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.509 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.685 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.682 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.569 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.539 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.598 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.581 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.587 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.539 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.700 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.740 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.404 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.559 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.650 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.535 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.599 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.700 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.570 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.560 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.643 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.580 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.642 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.547 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.630 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.634 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.604 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.713 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.593 |
MOD_N-GLC_1 | 626 | 631 | PF02516 | 0.671 |
MOD_N-GLC_1 | 67 | 72 | PF02516 | 0.594 |
MOD_N-GLC_2 | 255 | 257 | PF02516 | 0.630 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.514 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.627 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.575 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.615 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.553 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.706 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.668 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.565 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.636 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.551 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.501 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.731 |
MOD_PIKK_1 | 98 | 104 | PF00454 | 0.700 |
MOD_PKA_1 | 204 | 210 | PF00069 | 0.627 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.649 |
MOD_PKA_1 | 404 | 410 | PF00069 | 0.685 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.605 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.607 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.627 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.472 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.633 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.609 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.711 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.745 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.646 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.636 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.755 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.545 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.533 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.628 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.592 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.576 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.559 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.579 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.602 |
MOD_Plk_1 | 513 | 519 | PF00069 | 0.608 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.594 |
MOD_Plk_2-3 | 332 | 338 | PF00069 | 0.587 |
MOD_Plk_2-3 | 474 | 480 | PF00069 | 0.678 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.472 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.532 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.512 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.706 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.586 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.690 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.638 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.684 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.585 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.646 |
MOD_SUMO_rev_2 | 140 | 150 | PF00179 | 0.626 |
MOD_SUMO_rev_2 | 457 | 465 | PF00179 | 0.597 |
MOD_SUMO_rev_2 | 70 | 77 | PF00179 | 0.619 |
TRG_DiLeu_BaEn_2 | 279 | 285 | PF01217 | 0.523 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.655 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA33 | Leptomonas seymouri | 45% | 100% |
A4HJ28 | Leishmania braziliensis | 63% | 100% |
A4I6K7 | Leishmania infantum | 99% | 100% |
E9B1K0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q6L3 | Leishmania major | 92% | 100% |