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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: Q4Q5B0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.563 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.671 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.822 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.822 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.685 |
DEG_APCC_DBOX_1 | 83 | 91 | PF00400 | 0.671 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.692 |
DEG_SPOP_SBC_1 | 237 | 241 | PF00917 | 0.678 |
DOC_CKS1_1 | 301 | 306 | PF01111 | 0.726 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.638 |
DOC_CKS1_1 | 445 | 450 | PF01111 | 0.700 |
DOC_CYCLIN_RxL_1 | 89 | 100 | PF00134 | 0.534 |
DOC_MAPK_gen_1 | 132 | 141 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 134 | 143 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 483 | 492 | PF00069 | 0.580 |
DOC_PP1_RVXF_1 | 267 | 274 | PF00149 | 0.659 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.809 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.810 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.826 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.830 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.785 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 269 | 274 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 287 | 296 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.785 |
LIG_14-3-3_CanoR_1 | 364 | 372 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 499 | 506 | PF00244 | 0.788 |
LIG_Actin_WH2_2 | 271 | 289 | PF00022 | 0.693 |
LIG_Actin_WH2_2 | 340 | 357 | PF00022 | 0.664 |
LIG_deltaCOP1_diTrp_1 | 104 | 111 | PF00928 | 0.505 |
LIG_EH1_1 | 454 | 462 | PF00400 | 0.797 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.623 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.805 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.564 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.425 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.671 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.568 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.693 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.733 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.699 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.566 |
LIG_GBD_Chelix_1 | 139 | 147 | PF00786 | 0.428 |
LIG_LIR_Apic_2 | 291 | 296 | PF02991 | 0.803 |
LIG_LIR_Gen_1 | 108 | 118 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 231 | 238 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 350 | 359 | PF02991 | 0.660 |
LIG_LIR_Gen_1 | 375 | 383 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 375 | 379 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.775 |
LIG_LIR_Nem_3 | 480 | 485 | PF02991 | 0.698 |
LIG_MAD2 | 459 | 467 | PF02301 | 0.685 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.556 |
LIG_PCNA_yPIPBox_3 | 338 | 348 | PF02747 | 0.557 |
LIG_Pex14_1 | 111 | 115 | PF04695 | 0.610 |
LIG_Pex14_2 | 195 | 199 | PF04695 | 0.716 |
LIG_Pex14_2 | 372 | 376 | PF04695 | 0.650 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.611 |
LIG_SH2_CRK | 482 | 486 | PF00017 | 0.703 |
LIG_SH2_SRC | 206 | 209 | PF00017 | 0.725 |
LIG_SH2_STAT3 | 85 | 88 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.725 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.675 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.599 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.615 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.787 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.797 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.691 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.550 |
LIG_SUMO_SIM_par_1 | 397 | 403 | PF11976 | 0.746 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.668 |
LIG_UBA3_1 | 270 | 279 | PF00899 | 0.418 |
LIG_UBA3_1 | 399 | 407 | PF00899 | 0.650 |
LIG_WRC_WIRS_1 | 270 | 275 | PF05994 | 0.645 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.649 |
MOD_CDK_SPxK_1 | 444 | 450 | PF00069 | 0.821 |
MOD_CDK_SPxK_1 | 9 | 15 | PF00069 | 0.668 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.553 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.523 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.800 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.542 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.733 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.829 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.690 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.829 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.685 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.554 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.780 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.708 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.642 |
MOD_DYRK1A_RPxSP_1 | 444 | 448 | PF00069 | 0.708 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.495 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.636 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.619 |
MOD_GlcNHglycan | 328 | 332 | PF01048 | 0.552 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.447 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.541 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.573 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.751 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.817 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.770 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.506 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.578 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.637 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.512 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.727 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.664 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.505 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.808 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.668 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.770 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.643 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.803 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.672 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.561 |
MOD_LATS_1 | 277 | 283 | PF00433 | 0.556 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.793 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.718 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.482 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.724 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.680 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.487 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.702 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.549 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.784 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.668 |
MOD_PIKK_1 | 473 | 479 | PF00454 | 0.794 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.821 |
MOD_PK_1 | 417 | 423 | PF00069 | 0.744 |
MOD_PK_1 | 76 | 82 | PF00069 | 0.629 |
MOD_PKA_1 | 279 | 285 | PF00069 | 0.585 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.671 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.486 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.627 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.683 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.789 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.570 |
MOD_PKA_2 | 416 | 422 | PF00069 | 0.769 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.673 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.812 |
MOD_PKB_1 | 497 | 505 | PF00069 | 0.697 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.688 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.622 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.823 |
MOD_Plk_2-3 | 254 | 260 | PF00069 | 0.688 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.611 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.519 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.676 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.597 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.789 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.824 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.540 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.664 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.830 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.775 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.588 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.512 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.697 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.785 |
TRG_DiLeu_BaEn_1 | 180 | 185 | PF01217 | 0.729 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.552 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 395 | 400 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 44 | 49 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.702 |
TRG_ER_diArg_1 | 284 | 287 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 443 | 446 | PF00400 | 0.719 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 408 | 412 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.619 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H7S0 | Leishmania donovani | 86% | 100% |
A4HKF7 | Leishmania braziliensis | 67% | 100% |