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: E9AMS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 220 | 224 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.466 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 356 | 358 | PF00082 | 0.759 |
CLV_PCSK_PC1ET2_1 | 509 | 511 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.510 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.789 |
DEG_SCF_FBW7_1 | 374 | 381 | PF00400 | 0.708 |
DEG_SIAH_1 | 52 | 60 | PF03145 | 0.537 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.688 |
DOC_CKS1_1 | 375 | 380 | PF01111 | 0.774 |
DOC_CYCLIN_RxL_1 | 493 | 503 | PF00134 | 0.474 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 484 | 491 | PF00069 | 0.449 |
DOC_MAPK_NFAT4_5 | 484 | 492 | PF00069 | 0.456 |
DOC_PP1_RVXF_1 | 185 | 191 | PF00149 | 0.510 |
DOC_PP1_RVXF_1 | 495 | 502 | PF00149 | 0.553 |
DOC_PP1_SILK_1 | 260 | 265 | PF00149 | 0.628 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.768 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.739 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.672 |
LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 31 | 38 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.499 |
LIG_AP2alpha_1 | 210 | 214 | PF02296 | 0.434 |
LIG_APCC_ABBA_1 | 498 | 503 | PF00400 | 0.620 |
LIG_APCC_ABBAyCdc20_2 | 497 | 503 | PF00400 | 0.620 |
LIG_BIR_III_4 | 133 | 137 | PF00653 | 0.510 |
LIG_CtBP_PxDLS_1 | 439 | 443 | PF00389 | 0.647 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.629 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.615 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.585 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.629 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.643 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.669 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.773 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.450 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.503 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 332 | 341 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 453 | 464 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.482 |
LIG_Pex14_2 | 210 | 214 | PF04695 | 0.525 |
LIG_RPA_C_Fungi | 488 | 500 | PF08784 | 0.362 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.464 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.689 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.571 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.557 |
LIG_SH3_3 | 372 | 378 | PF00018 | 0.666 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.495 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.683 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.559 |
LIG_SH3_CIN85_PxpxPR_1 | 273 | 278 | PF14604 | 0.527 |
LIG_SUMO_SIM_par_1 | 438 | 444 | PF11976 | 0.643 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.682 |
LIG_TRAF2_1 | 466 | 469 | PF00917 | 0.359 |
MOD_CDC14_SPxK_1 | 415 | 418 | PF00782 | 0.445 |
MOD_CDK_SPK_2 | 155 | 160 | PF00069 | 0.622 |
MOD_CDK_SPK_2 | 254 | 259 | PF00069 | 0.660 |
MOD_CDK_SPK_2 | 412 | 417 | PF00069 | 0.458 |
MOD_CDK_SPxK_1 | 412 | 418 | PF00069 | 0.459 |
MOD_CDK_SPxxK_3 | 191 | 198 | PF00069 | 0.512 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.693 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.767 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.732 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.751 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.508 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.592 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.747 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.731 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.768 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.666 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.666 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.727 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.588 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.615 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.490 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.750 |
MOD_Cter_Amidation | 196 | 199 | PF01082 | 0.520 |
MOD_DYRK1A_RPxSP_1 | 155 | 159 | PF00069 | 0.713 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.770 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.677 |
MOD_GlcNHglycan | 138 | 142 | PF01048 | 0.733 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.697 |
MOD_GlcNHglycan | 272 | 276 | PF01048 | 0.704 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.702 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.618 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.601 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.642 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.431 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.555 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.706 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.542 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.704 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.679 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.653 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.721 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.492 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.703 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.596 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.492 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.512 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.588 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.576 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.550 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.588 |
MOD_PKB_1 | 187 | 195 | PF00069 | 0.623 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.735 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.556 |
MOD_Plk_2-3 | 180 | 186 | PF00069 | 0.537 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.628 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.608 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.500 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.548 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.437 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.367 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.690 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.510 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.567 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.691 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.739 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.459 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.678 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.654 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.673 |
MOD_SUMO_for_1 | 355 | 358 | PF00179 | 0.756 |
MOD_SUMO_rev_2 | 60 | 68 | PF00179 | 0.544 |
TRG_DiLeu_BaEn_4 | 315 | 321 | PF01217 | 0.683 |
TRG_DiLeu_LyEn_5 | 503 | 508 | PF01217 | 0.620 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 303 | 307 | PF00026 | 0.696 |
TRG_Pf-PMV_PEXEL_1 | 31 | 35 | PF00026 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 318 | 323 | PF00026 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILK1 | Leptomonas seymouri | 37% | 98% |
A0A3S7WQP0 | Leishmania donovani | 88% | 100% |
A4H5Q2 | Leishmania braziliensis | 71% | 100% |
A4HTZ2 | Leishmania infantum | 88% | 100% |
Q4QHV3 | Leishmania major | 85% | 100% |